4-oxoquinoline-3-carboxylic acid derivatives their preparation and their use

ABSTRACT

Compounds of formula (I):   &lt;IMAGE&gt; (I)  (in which: R1 represents fluorinated methoxy: R2 represents a nitrogen-containing heterocyclic group and R3 represents hydrogen or amino) and pharmaceutically acceptable salts, esters and amides thereof are valuable antibacterial agents, which may be prepared by reacting a compound similar to that of formula (I) but in which R2 is replaced by a halogen atom with a compound providing the required group R2.

This is a division of application Ser. No. 08/227,678 filed Apr. 14, 1994, now U.S. Pat. No. 5,436,367, which is a division of Ser. No. 07/594,283 filed Oct. 9, 1990, now U.S. Pat. No. 5,348,961, which is a division of application Ser. No. 07/381,025 filed Jul. 17, 1989, now abandoned.

BACKGROUND OF THE INVENTION

The present invention relates to a series of novel 8-(fluorinated methoxy)-4-oxoquinoline-carboxylic acid derivatives which have been found to have valuable and powerful antibacterial activity. The invention also provides compositions containing these compounds, methods of using them and processes for preparing them.

The compounds of the present invention are 1-cyclopropyl-4-oxo-6-fluoro-7-(optionally substituted heterocyclic)-8-(fluorinated methoxy)-quinoline-3-carboxylic acid derivatives and 1-cyclopropyl-4-oxo-5-amino-6-fluoro-7-(optionally substituted heterocyclic)-8-(fluorinated methoxy)-quinoline-3-carboxylic acid derivatives.

It is an unfortunate fact of modern medicine that many infectious bacteria are gradually developing resistance to the antibiotics commonly Used to treat infection caused by them, with the result that known antibacterial agents are increasingly becoming of limited effectiveness. There is, therefore, a continuing need to develop new antibacterial agents, which may, even if only for a restricted period, be effective against infectious bacteria. Most of the common antibacterial agents in present day use were originally developed from fermentation products, although some are of wholly synthetic origin.

There have been proposals to use certain 4-oxoquinoline-3-carboxylic acid derivatives as antibacterial agents. For example, European Patent Publication No. 78 362 discloses a limited class of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)quinoline-3-carboxylic acid derivatives, in which the piperazinyl group is unsubstituted or has a methyl, ethyl or β-hydroxyethyl substituent at the 4-position. These compounds resemble certain of those of the present invention, except that they lack the 8-fluorinated methoxy group which has been found to be critical to the achievement of the excellent activity of the compounds of the present invention.

European Patent Publications No. 106 489, No. 153 163. No. 230 295, No. 235 762 and No. 241 206 disclose classes of quinoline derivatives, including amongst many others, some 1-substituted-4-oxo-1,4-dihydro-6-halo-7-(optionally substituted heterocyclic)-8-substituted-quinoline-3-carboxylic acid derivatives, of which in some the 8-substituent is an alkoxy group, but do not disclose any compounds in which the 8-substituent is a fluorinated methoxy group. Of the compounds disclosed in European Patent Publication No. 78 362, one, namely Norfloxacin, whose systematic name is 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-quinoline-3-carboxylic acid, is disclosed in The Merck Index Tenth Edition, published in 1983, monograph number 6541. In common with the other compounds of European Patent Publication No 78 362, this lacks the critical 8-fluorinated methoxy substituent of the present invention.

We have surprisingly found that the combination of a limited class of 8-fluorinated methoxy substituents with certain limited and highly specific classes of heterocyclic substituent at the 7-position and optionally an amino group at the 5-position leads to the production of compounds which have unexpectedly good antibacterial activities against Gram positive and Gram negative bacteria, in many cases far surpassing those of the prior art compounds. In particular, the compounds of the present invention have surprisingly good activity against several Gram positive bacteria against which the known compounds are ineffective or are effective only at high concentrations, for example Staphylococcus aureus and Enterococcus faecalis.

It is believed that the closest prior art is the aforementioned European Patent Publications No. 78 362, No. 230 295 and No. 241 206. We have surprisingly found that the compounds of the present invention show an exceptional antibacterial activity against penicillin- and cephalosporin- resistant Gram positive bacteria and Pseudomonas aeruginosa, which can be controlled only with difficulty with β-lactam antibiotics, and which are, therefore, a major problem in medicine.

BRIEF SUMMARY OF INVENTION

It is, therefore, an object of the present invention to provide a series of 1,4-dihydro-4-oxoquinoline-3-carboxylic acid derivatives which have exceptional antibacterial activity.

It is a further object of the invention to provide pharmaceutical compositions containing such a quinoline derivative as an antibacterial agent.

It is a still further object of the present invention to provide methods for the treatment or prophylaxis of bacterial infections in animals (including human beings) by the administration thereto of such a quinoline derivative.

The compounds of the present invention are those compounds of formula (I): ##STR2## in which

R¹ represents a methoxy group having at least one fluorine substituent:

R² represents a group selected from the group consisting of:

(i) groups of formula (II) ##STR3## in which: R⁴ represents a hydrogen atom; a hydroxy group; an amino group; a C₁ -C₆ alkyl group; a substituted C₁ -C₆ alkyl group having at least one substituent selected from the group consisting of substituents (a), defined below; an aralkyl group; a C₁ -C₆ aliphatic acyl group; or a substituted C₂ -C₆ aliphatic acyl group having at least one substituent selected from the group consisting of substituents (a), defined below;

R⁵ represents a hydrogen atom, a C₁ -C₆ alkyl group or a substituted C₁ -C₆ alkyl group having at least one substituent selected from the group consisting of substituents (b), defined below;

A represents an ethylene group, a trimethylene group, or a group of formula --COCH₂ --, and

m represents 1 or 2;

(ii) groups of formula (III): ##STR4## in which: R⁶ represents a hydrogen atom; a C₁ -C₆ alkyl group; a substituted C₁ -C₆ alkyl group having at least one substituent selected from the group consisting of substituents (b), defined below; a hydroxy group; a C₁ -C₆ alkoxy group; or a C₁ -C₆ alkoxy group having at least one fluorine substituent;

R⁷ represents a group of formula R⁸ R⁹ N--(CH₂)_(q) --, in which R⁸ and R⁹ are independently selected from the group consisting of hydrogen atoms. C₁ -C₆ alkyl groups and aralkyl groups, and q represents 0 or 1; a hydroxy group; or a C₁ -C₆ alkoxy group;

B represents a methylene group, an ethylene group, a trimethylene group, or a tetramethylene group; and

n represents 1 or 2;

(iii) groups of formula (IV): ##STR5## in which: R¹⁰ represents a hydrogen atom or a C₁ -C₆ alkyl group; and

(iv) groups of formula (V): ##STR6## in which: Z represents a oxygen atom or a sulfur atom;

R³ represents a hydrogen atom or an amino group;

substituents (a):

hydroxy groups, C₁ -C₆ alkoxy groups, C₂ -C₆ aliphatic acyloxy groups, C₁ -C₆ aliphatic acyl groups, carboxy groups, C₂ -C₆ alkoxycarbonyl groups, sulfo groups, amino groups, C₂ -C₆ aliphatic acylamino groups, and mono- and di-(C₁ -C₆ alkyl) substituted amino groups;

substituents (b):

hydroxy groups, C₁ -C₆ alkoxy groups, and halogen atoms; and

said aralkyl groups have from 1 to 4 carbon atoms in the alkyl part and have an aryl part which has from 6 to 10 carbon atoms and which is unsubstituted or has at least one substituent selected from the group consisting of substituents (c), defined below;

substituents (c):

hydroxy groups, C₁ -C₆ alkyl groups, C₁ -C₆ alkoxy groups, C₂ -C₆ aliphatic acyloxy groups, C₁ -C₆ aliphatic acyl groups, carboxy groups, C₂ -C₆ alkoxycarbonyl groups, sulfo groups, nitro groups, cyano groups, amino groups, C₂ -C₆ aliphatic acylamino groups, and mono- and di-(C₁ -C₆ alkyl) substituted amino groups;

and pharmaceutically acceptable salts, esters and amides thereof.

The invention also provides a pharmaceutical composition for the treatment of bacterial infections, comprising an effective amount of an antibacterial agent in combination with a pharmaceutically acceptable carrier or diluent, wherein the antibacterial agent is selected from the group consisting of compounds of formula (I) and pharmaceutically acceptable salts, esters and amides thereof.

The invention still further provides a method for the treatment or prophylaxis of bacterial infection comprising administering an amount of an antibacterial agent to an animal (which may be a mammal, e.g. human) sufficient to exert an antibacterial effect, wherein said antibacterial agent is selected from the group consisting of compounds of formula (I) and pharmaceutically acceptable salts, esters and amides thereof.

The invention also provides methods of preparing the compounds of the invention, which are described in more detail hereafter.

DETAILED DESCRIPTION OF INVENTION

In the compounds of the present invention, R¹ represents a methoxy group having at least one fluorine substituent, which may be a monofluoromethoxy group, a difluoromethoxy group or a trifluoromethoxy group of which the difluoromethoxy and trifluoromethoxy groups are preferred.

Where R² represents a group of formula (II) and R⁴ represents an alkyl group, this may be a straight or branched chain alkyl group containing from 1 to 6, preferably from 1 to 4, carbon atoms, and examples of such groups include the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, isopentyl, t-pentyl, hexyl and 1,3-dimethylbutyl groups. Of these, the methyl, ethyl, propyl, isopropyl, butyl and isobutyl groups are preferred. Such alkyl groups may be unsubstituted or may have at least one substituent selected from the group consisting of substituents (a), defined above, that is:

hydroxy groups;

straight and branched chain alkoxy groups containing from 1 to 6, preferably from 1 to 3, carbon atoms such as the methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, pentyloxy, isopentyloxy, t-pentyloxy and hexyloxy groups. Of these, the methoxy, ethoxy, propoxy and isopropoxy groups are preferred;

aliphatic acyloxy groups containing from 2 to 6, preferably from 2 to 4, carbon atoms such as the acetoxy, propionyloxy, butyryloxy, isobutyryloxy, valeryloxy, isovaleryloxy, pivaloyloxy and hexanoyloxy groups, of which the acetoxy, propionyloxy, butyryloxy and isobutyryloxy groups are preferred;

aliphatic acyl groups containing from 1 to 6, preferably from 1 to 4, carbon atoms such as the formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl and hexanoyl groups, of which the formyl, acetyl, propionyl, butyryl and isobutyryl groups are preferred;

carboxy groups;

alkoxycarbonyl groups containing a total of from 2 to 6, preferably from 2 to 4, carbon atoms (i.e. the alkoxy part has from 1 to 5, preferably from 1 to 3, carbon atoms), such as the methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl, t-butoxycarbonyl and pentyloxycarbonyl groups, of which the methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl and isopropoxycarbonyl groups are preferred;

sulfo groups;

amino groups;

aliphatic acylamino groups containing from 2 to 6, preferably from 2 to 4, carbon atoms such as acetoamido, propionamido, butyramido, isobutyramido, valeramido, isovaleramido and pivaloylamino groups, of which the acetoamido, propionamido, butyramido and isobutyramido groups are preferred; and

mono- and di-alkyl-substituted amino groups in which the or each alkyl group contains from 1 to 6, preferably from 1 to 4, carbon atoms such as the methylamino, ethylamino, propylamino, isopropylamino, butylamino, isobutylamino, dimethylamino, diethylamino, dipropylamino, diisopropylamino, pentylamino and hexylamino groups, of which the methylamino, dimethylamino, ethylamino, propylamino, isopropylamino, butylamino and isobutylamino groups are preferred.

Where R⁴ represents an aralkyl group, this has from 1 to 4 alkyl groups in the alkyl part and from 6 to 10 carbon atoms in the aryl part. Examples of such groups include the benzyl, phenethyl, 1-phenylethyl, 1-phenylpropyl, 2-phenylpropyl, 3-phenylpropyl, 4-phenylbutyl, 1-naphthylmethyl and 2-naphthylmethyl groups. These groups may be unsubstituted or may have at least one substituent on the aryl part selected from the group consisting of substituents (c), defined above. Examples of the groups which may be included in substituents (c) are as exemplified in relation to the same groups included in substituents (a), as well as C₁ -C₆ alkyl groups, such as those exemplified in relation to the alkyl groups which may be represented by R⁴ nitro groups and cyano groups especially alkoxy groups, amino groups and mono- and di- alkylamino groups. Examples of such groups include the benzyl, p-methoxybenzyl, p-aminobenzyl, p-methylaminobenzyl and p-dimethylaminobenzyl groups.

Where R⁴ represents an aliphatic acyl group, this may contain from 1 to 6, preferably from 1 to 4, carbon atoms, and examples include the formyl, acetyl, propionyl, butyryl, isobutyryl, valeryl, isovaleryl, pivaloyl and hexanoyl groups, of which the formyl, acetyl, propionyl, butyryl and isobutyryl groups are preferred. These groups may be unsubstituted or may have at least one substituent selected from the group consisting of substituents (a), defined and exemplified above.

Where R² represents said group of formula (II) or said group of formula (IV), R⁵ and R¹⁰, respectively, may each represent a hydrogen atom or an alkyl group containing from 1 to 6, preferably from 1 to 3, carbon atoms. Examples of such groups include the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, isopentyl, t-pentyl, hexyl and 1,3-dimethylbutyl groups. Of these, the methyl, ethyl, propyl and isopropyl groups are preferred. R⁵ may also represent such an alkyl group having at least one substituent selected from the group consisting of substituents (b), defined above, i.e.:

hydroxy groups;

straight and branched chain alkoxy groups containing from 1 to 6, preferably from 1 to 3, carbon atoms such as the methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, pentyloxy, isopentyloxy, t-pentyloxy and hexyloxy groups. Of these, the methoxy, ethoxy, propoxy and isopropoxy groups are preferred; and

halogen atoms, such as the fluorine, chlorine, bromine and iodine atoms, of which the fluorine and chlorine atoms are preferred.

Where R² represents said group of formula (III), R⁶ may represent: a hydrogen atom; an alkyl group containing from 1 to 6, preferably from 1 to 3, carbon atoms, such as the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, isopentyl, t-pentyl, hexyl and 1,3-dimethylbutyl groups, of which the methyl, ethyl, propyl and isopropyl groups are preferred; a substituted alkyl group having from 1 to 6 carbon atoms, which may be any of the unsubstituted groups exemplified above and in which the substituent is selected from the group consisting of substituents (b), defined and exemplified above; a hydroxy group; an alkoxy group containing from 1 to 6, preferably from 1 to 3, carbon atoms, such as the methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, pentyloxy, isopentyloxy, t-pentyloxy and hexyloxy groups, of which the methoxy, ethoxy, propoxy and isopropoxy groups are preferred; or an alkoxy group containing from 1 to 6, preferably from 1 to 3, carbon atoms and having at least one fluorine substituent, such as the fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy, 2,2,2-trifluoroethoxy, 3-fluoropropoxy, 4-fluorobutoxy, 5-fluoropentyloxy, 6-fluorohexyloxy, 3,3-difluoropropoxy, 3,3,3-trifluoropropoxy, 4,4-difluorobutoxy and 4,4,4-trifluorobutoxy groups, of which the fluoromethoxy, difluoromethoxy, trifluoromethoxy, 1-fluoroethoxy, 2-fluoroethoxy, 2,2-difluoroethoxy and 2,2,2-trifluoroethoxy groups are preferred.

Where R² represents said group of formula (III) and R⁷ represents said group of formula R⁸ R⁹ N--(CH₂)_(q) --, R⁸ and R⁹ may be the same or different and each represents; a hydrogen atom: an alkyl group containing from 1 to 6, preferably from 1 to 3, carbon atoms, such as the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, isopentyl, t-pentyl, hexyl and 1,3-dimethylbutyl groups, of which the methyl, ethyl, propyl and isopropyl groups are preferred; or an aralkyl group, which may be as defined and exemplified above in relation to the aralkyl groups which may be represented by R⁴, and may optionally be substituted by at least one substituent selected from the group consisting of substituents (c), defined and exemplified above, and preferably with a C₁ -C₆ alkoxy group, an amino group, or a mono- or di-(C₁ -C₆) alkylamino group such as the benzyl, p-methoxybenzyl, p-aminobenzyl, p-methylaminobenzyl and p-dimethylaminobenzyl groups.

Alternatively, R⁷ may represent: a hydroxy group; or an alkoxy group containing from 1 to 6, preferably from 1 to 3, carbon atoms such as the methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, pentyloxy, isopentyloxy, t-pentyloxy and hexyloxy groups, of which the methoxy, ethoxy, propoxy and isopropoxy groups are preferred.

In the group of formula (V), Z may be an oxygen atom or a sulfur atom; where it is an oxygen atom, the group is the morpholino group; where it is a sulfur atom, the group is a thiomorpholino (i.e. perhydro-1,4-thiazin-4-yl) group.

Of the compounds of formula (I), the preferred compounds are those in which R² represents:

a group of formula (II): ##STR7## (in which R⁴, R⁵, A and m are as defined above); a group of formula (IIIa): ##STR8## (in which: R^(6') represents a hydrogen atom or an alkyl group having from 1 to 3 carbon atoms; B' represents a methylene group or an ethylene group; and n is as defined above);

a group of formula (IIIb): ##STR9## (in which R⁶, R⁸, R⁹, B', n and q are as defined above); a group of formula (IIIc): ##STR10## (in which: R¹¹ and R¹² are independently selected from the group consisting of hydroxy groups and alkoxy groups having from 1 to 3 carbon atoms);

a group of formula (IVa): ##STR11## (in which R¹⁰ is as defined above); or a group of formula (V): ##STR12## (in which Z is as defined above).

We also prefer those compounds of formula (I) in which R¹ represents a difluoromethoxy group or a trifluoromethoxy group, and especially those in which R¹ represents a difluoromethoxy group or a trifluoromethoxy group and R² represents a group of formula (II), (IIIa), (IIIb), (IIIc), (IVa) or (V), as defined above, both where R³ represents a hydrogen atom and where it represents an amino group.

The compounds of the invention contain one carboxy group at the 3-position of the quinoline ring. This carboxy group may form esters, amides and salts.

Where the carboxy group is esterified, the nature of the resulting ester is not critical to the present invention. In principle, the compounds of the invention, being carboxylic acids, will form esters with any ester-forming alcohol and all such esters form part of the present invention. However, where the esters are to be employed for therapeutic purposes, it is, of course, necessary that the resulting esters should be pharmaceutically acceptable, which, as is well understood in the art, means that the esters should not have reduced activity (or unacceptably reduced activity) and should not have increased toxicity (or unacceptably increased toxicity) as compared with the free acid. However, where the ester is to be employed for other purposes, for example as an intermediate in the preparation of other compounds, even this criterion does not apply.

Examples of such esters include: C₁ -C₆, more preferably C₁ -C₄, alkyl esters, for example the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, t-butyl, pentyl and hexyl esters; aralkyl (including diarylalkyl) esters, such as the benzyl, p-nitrobenzyl and benzhydryl esters; lower aliphatic acyloxyalkyl groups, such as the acetoxymethyl or pivaloyloxymethyl groups; alkoxycarbonylalkyl esters, in which the alkoxy and alkyl parts are both C₁ -C₄, especially alkoxycarbonylmethyl and 1-(alkoxycarbonyl)ethyl esters, such as the ethoxycarbonylmethyl and t-butoxycarbonylmethyl esters; alkoxycarbonyloxyalkyl esters in which the alkoxy and alkyl parts are both C₁ -C₄, especially the 1- and 2-(alkoxycarbonyloxy)ethyl esters, such as the 1-(ethoxycarbonyloxy)ethyl, 1-(isopropoxycarbonyloxy)ethyl, 2-methoxycarbonyloxyethyl, 2-ethoxycarbonyloxyethyl and 2-t-butoxycarbonyloxyethyl esters; N,N-di-substituted aminocarbonylalkyl esters, in which the alkyl group is C₁ -C₆ , preferably C₁ -C₄, and the substituents on the amino group are preferably C₁ -C₄ alkyl groups such as the N,N-dimethylaminocarbonylmethyl esters; and other specific esters, such as the phthalidyl, substituted phthalidyl, phenacyl, substituted phenacyl (e.g. p-nitrophenacyl), (5-phenyl-2-oxo-1,3-dioxolen-4-yl)methyl and (5-methyl-2-oxo-1,3-dioxolen-4-yl)methyl esters.

Likewise, where the carboxy group has formed an amide, the precise nature of the amide is not critical, provided that, where the amide is to be used for therapeutic purposes, the resulting amide is pharmaceutically acceptable. Accordingly, the carboxy group can be replaced by a carbamoyl group or a substituted carbamoyl group, preferably an alkylcarbamoyl or dialkylcarbamoyl group in which the or each alkyl group is a C₁ -C₃ alkyl group (e.g. as defined above in relation to R⁴), for example a methylcarbamoyl, ethylcarbamoyl, dimethylcarbamoyl or diethylcarbamoyl group.

The carboxy group may also form salts with appropriate bases. The nature of such salts is likewise not critical, provided that, where they are to be used for therapeutic purposes, the salts are pharmaceutically acceptable. Examples of salts with bases include: salts with metals, especially alkali metals and alkaline earth metals, such as lithium, sodium, potassium, calcium and magnesium, and other metals, such as manganese, iron and aluminum; the ammonium salt; salts with organic amines, such as cyclohexylamine, diisopropylamine or triethylamine; and salts with basic amino acids, such as lysine or arginine.

The compounds of the invention contain a basic nitrogen atom and hence can also form acid addition salts. The nature of such salts is likewise not critical to the present invention, except that, where the salts are to be used for therapeutic purposes, they must be pharmaceutically acceptable. A wide variety of acids may be employed to form such salts and representative examples of such acids include: mineral acids, such as hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid, metaphosphoric acid, nitric acid or sulfuric acid; organic carboxylic acids, such as acetic acid, oxalic acid, tartaric acid, citric acid, benzoic acid, glycolic acid, gluconic acid, glucuronic acid, succinic acid, maleic acid or fumaric acid; and organic sulfonic acids, such as methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid or p-toluenesulfonic acid. Such acid addition salts may be prepared by conventional methods.

The compounds of the invention may also exist in the form of hydrates and these likewise form part of the present invention.

Specific examples of compounds of the invention are given by the foregoing formula (I), in which the substituents are as defined in the following Table 1. In the Table, the following abbreviations are used:

                  TABLE 1     ______________________________________     Cpd     No.   R.sup.1   R.sup.3 R.sup.2     ______________________________________      1    OCHF.sub.2                     H       1-Piz      2    OCHF.sub.2                     H       3-Me-1-Piz      3    OCHF.sub.2                     H       3,5-diMe-1-Piz      4    OCHF.sub.2                     H       2,5-diMe-1-Piz      5    OCHF.sub.2                     H       4-Me-1-Piz      6    OCHF.sub.2                     H       3,4-diMe-1-Piz      7    OCHF.sub.2                     H       3,4,5-triMe-1-Piz      8    OCHF.sub.2                     H       4-Et-1-Piz      9    OCHF.sub.2                     H       4-(2-HOEt)-1-Piz     10    OCHF.sub.2                     H       4-(2-MeOEt)-1-Piz     11    OCHF.sub.2                     H       4-(2-AcOEt)-1-Piz     12    OCHF.sub.2                     H       4-(2-NH.sub.2 Et)-1-Piz     13    OCHF.sub.2                     H       4-(2-NMe.sub.2 Et)-1-Piz     14    OCHF.sub.2                     H       4-(4-NH.sub.2 Bz)-1-Piz     15    OCHF.sub.2                     H       4-HCO-1-Piz     16    OCHF.sub.2                     H       4-Ac-1-Piz     17    OCHF.sub.2                     H       4-(AcMe)-1-Piz     18    OCHF.sub.2                     H       4-(EtcMe)-1-Piz     19    OCHF.sub.2                     H       4-(SfoMe)-1-Piz     20    OCHF.sub.2                     H       1-Diz     21    OCHF.sub.2                     H       4-Me-1-Diz     22    OCHF.sub.2                     H       3-oxo-1-Piz     23    OCHF.sub.2                     H       4-Me-3-oxo-1-Piz     24    OCHF.sub.2                     H       3-HO-1-Pyrd     25    OCHF.sub.2                     H       4-HO-1-Pip     26    OCHF.sub.2                     H       3,4-diHO-1-Pyrd     27    OCHF.sub.2                     H       3-HO-4-MeO-1-Pyrd     28    OCHF.sub.2                     H       3-NH.sub.2 -1-Azt     29    OCHF.sub.2                     H       3-NHMe-1-Azt     30    OCHF.sub.2                     H       3-NMe.sub.2 -1-Azt     31    OCHF.sub.2                     H       3-(NH.sub.2 Me)-1-Azt     32    OCHF.sub.2                     H       3-[(NHEt)Me]-1-Azt     33    OCHF.sub.2                     H       3-[(NMe.sub.2)Me]-1-Azt     34    OCHF.sub.2                     H       3-NH.sub.2 -1-Pyrd     35    OCHF.sub.2                     H       3-NHEt-1-Pyrd     36    OCHF.sub.2                     H       3-NMe.sub.2 -1-Pyrd     37    OCHF.sub.2                     H       3-(NH.sub.2 Me)-1-Pyrd     38    OCHF.sub.2                     H       3-[(NHMe)Me]-1-Pyrd     39    OCHF.sub.2                     H       3-[(NHEt)Me]-1-Pyrd     40    OCHF.sub.2                     H       3-[(NMe.sub.2)Me]-1-Pyrd     41    OCHF.sub.2                     H       3-NH.sub.2 -4-Me-1-Pyrd     42    OCHF.sub.2                     H       3-NH.sub.2 -4-HO-1-Pyrd     43    OCHF.sub.2                     H       3-NH.sub.2 -4-MeO-1-Pyrd     44    OCHF.sub.2                     H       3-NH.sub.2 -4-EtO-1-Pyrd     45    OCHF.sub.2                     H       4-NH.sub.2 -1-Pip     46    OCHF.sub.2                     H       4-NHMe-1-Pip     47    OCHF.sub.2                     H       4-NMe.sub.2 -1-Pip     48    OCHF.sub.2                     H       3-NH.sub.2 -1-Pip     49    OCHF.sub.2                     H       3-NHMe-1-Pip     50    OCHF.sub.2                     H       3-NH.sub.2 -1-Azp     51    OCHF.sub.2                     H       3-NH.sub.2 -3-Me-1-Pyrd     52    OCHF.sub.2                     H       1-Imid     53    OCHF.sub.2                     H       4-Me-1-Imid     54    OCHF.sub.2                     H       Mor     55    OCHF.sub.2                     H       Thz     56    OCHF.sub.2                     H       3-Et-1-Piz     57    OCHF.sub.2                     H       3,3-diMe-1-Piz     58    OCHF.sub.2                     H       3-iPr-1-Piz     59    OCHF.sub.2                     H       3-(MeOMe)-1-Piz     60    OCHF.sub.2                     H       4-(HCOMe)-3-Me-1-Piz     61    OCHF.sub.2                     H       3,5-di(CH.sub.2 F)-1-Piz     62    OCHF.sub.2                     H       4-NH.sub.2 -1-Piz     63    OCHF.sub.2                     H       4-HO-1-Piz     64    OCHF.sub.2                     H       4-(2-HOEt)-3-Me-1-Piz     65    OCHF.sub.2                     H       4-(2-MeOEt)-3-Me-1-Piz     66    OCHF.sub.2                     H       3-CH.sub.2 F-1-Piz     67    OCHF.sub.2                     H       4-NH.sub.2 -3-Me-1-Piz     68    OCHF.sub.2                     H       4-(HCOMe)-1-Piz     69    OCHF.sub.2                     H       4-HO-3-Me-1-Piz     70    OCHF.sub.2                     H       4-(AcMe)-3-Me-1-Piz     71    OCHF.sub.2                     H       3-Me-1-Diz     72    OCHF.sub.2                     H       3-NH.sub.2 -4-(MeOMe)-1-Pyrd     73    OCHF.sub.2                     H       3-NH.sub.2 -4-(CF.sub.3 CH.sub.2 O)-1-Pyrd     74    OCHF.sub.2                     NH.sub.2                             1-Piz     75    OCHF.sub.2                     NH.sub.2                             3-Me-1-Piz     76    OCHF.sub.2                     NH.sub.2                             3,5-diMe-1-Piz     77    OCHF.sub.2                     NH.sub.2                             2,5-diMe-1-Piz     78    OCHF.sub.2                     NH.sub.2                             4-Me-1-Piz     79    OCHF.sub.2                     NH.sub.2                             3,4-diMe-1-Piz     80    OCHF.sub.2                     NH.sub.2                             3,4,5-triMe-1-Piz     81    OCHF.sub.2                     NH.sub.2                             4-Et-1-Piz     82    OCHF.sub.2                     NH.sub.2                             4-(2-HOEt)-1-Piz     83    OCHF.sub.2                     NH.sub.2                             4-(2-MeOEt)-1-Piz     84    OCHF.sub.2                     NH.sub.2                             4-(2-AcOEt)-1-Piz     85    OCHF.sub.2                     NH.sub.2                             4-(2-NH.sub.2 Et)-1-Piz     86    OCHF.sub.2                     NH.sub.2                             4-(2-NMe.sub.2 Et)-1-Piz     87    OCHF.sub.2                     NH.sub.2                             4-(4-NH.sub.2 Bz)-1-Piz     88    OCHF.sub.2                     NH.sub.2                             4-HCO-1-Piz     89    OCHF.sub.2                     NH.sub.2                             4-Ac-1-Piz     90    OCHF.sub.2                     NH.sub.2                             4-(AcMe)-1-Piz     91    OCHF.sub.2                     NH.sub.2                             4-(EtcMe)-1-Piz     92    OCHF.sub.2                     NH.sub.2                             4-(SfoMe)-1-Piz     93    OCHF.sub.2                     NH.sub.2                             1-Diz     94    OCHF.sub.2                     NH.sub.2                             4-Me-1-Diz     95    OCHF.sub.2                     NH.sub.2                             3-oxo-1-Piz     96    OCHF.sub.2                     NH.sub.2                             4-Me-3-oxo-1-Piz     97    OCHF.sub.2                     NH.sub.2                             3-HO-1-Pyrd     98    OCHF.sub.2                     NH.sub.2                             4-HO-1-Pip     99    OCHF.sub.2                     NH.sub.2                             3,4-diHO-1-Pyrd     100   OCHF.sub.2                     NH.sub.2                             3-HO-4-MeO-1-Pyrd     101   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -1-Azt     102   OCHF.sub.2                     NH.sub.2                             3-NHMe-1-Azt     103   OCHF.sub.2                     NH.sub.2                             3-NMe.sub.2 -1-Azt     104   OCHF.sub.2                     NH.sub.2                             3-(NH.sub.2 Me)-1-Azt     105   OCHF.sub.2                     NH.sub.2                             3-[(NHEt)Me]-1-Azt     106   OCHF.sub.2                     NH.sub.2                             3-[(NMe.sub.2)Me]-1-Azt     107   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -1-Pyrd     108   OCHF.sub.2                     NH.sub.2                             3-NHEt-1-Pyrd     109   OCHF.sub.2                     NH.sub.2                             3-NMe.sub.2 -1-Pyrd     110   OCHF.sub.2                     NH.sub.2                             3-(NH.sub.2 Me)-1-Pyrd     111   OCHF.sub.2                     NH.sub.2                             3-[(NHMe)Me]-1-Pyrd     112   OCHF.sub.2                     NH.sub.2                             3-[(NHEt)Me]-1-Pyrd     113   OCHF.sub.2                     NH.sub.2                             3-[(NMe.sub.2)Me]-1-Pyrd     114   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -4-Me-1-Pyrd     115   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -4-HO-1-Pyrd     116   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -4-MeO-1-Pyrd     117   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -4-EtO-1-Pyrd     118   OCHF.sub.2                     NH.sub.2                             4-NH.sub.2 -1-Pip     119   OCHF.sub.2                     NH.sub.2                             4-NHMe-1-Pip     120   OCHF.sub.2                     NH.sub.2                             4-NMe.sub.2 -1-Pip     121   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -1-Pip     122   OCHF.sub.2                     NH.sub.2                             3-NHMe-1-Pip     123   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -1-Azp     124   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -3-Me-1-Pyrd     125   OCHF.sub.2                     NH.sub.2                             1-Imid     126   OCHF.sub.2                     NH.sub.2                             4-Me-1-Imid     127   OCHF.sub.2                     NH.sub.2                             Mor     128   OCHF.sub.2                     NH.sub.2                             Thz     129   OCHF.sub.2                     NH.sub.2                             3-Et-1-Piz     130   OCHF.sub.2                     NH.sub.2                             3,3-diMe-1-Piz     131   OCHF.sub.2                     NH.sub.2                             3-iPr-1-Piz     132   OCHF.sub.2                     NH.sub.2                             3-(MeOMe)-1-Piz     133   OCHF.sub.2                     NH.sub.2                             4-(HCOMe)-3-Me-1-Piz     134   OCHF.sub.2                     NH.sub.2                             3,5-di(CH.sub.2 F)-1-Piz     135   OCHF.sub.2                     NH.sub.2                             4-NH.sub.2 -1-Piz     136   OCHF.sub.2                     NH.sub.2                             4-HO-1-Piz     137   OCHF.sub.2                     NH.sub.2                             4-(2-HOEt)-3-Me-1-Piz     138   OCHF.sub.2                     NH.sub.2                             4-(2-MeOEt)-3-Me-1-Piz     139   OCHF.sub.2                     NH.sub.2                             3-CH.sub.2 F-1-Piz     140   OCHF.sub.2                     NH.sub.2                             4-NH.sub.2 -3-Me-1-Piz     141   OCHF.sub.2                     NH.sub.2                             4-(HCOMe)-1-Piz     142   OCHF.sub.2                     NH.sub.2                             4-HO-3-Me-1-Piz     143   OCHF.sub.2                     NH.sub.2                             4-(AcMe)-3-Me-1-Piz     144   OCHF.sub.2                     NH.sub.2                             3-Me-1-Diz     145   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -4-(MeOMe)-1-Pyrd     146   OCHF.sub.2                     NH.sub.2                             3-NH.sub.2 -4-(CF.sub.3 CH.sub.2 O)-1-Pyrd     147   OCF.sub.3 H       1-Piz     148   OCF.sub.3 H       3-Me-1-Piz     149   OCF.sub.3 H       3,5-diMe-1-Piz     150   OCF.sub.3 H       2,5-diMe-1-Piz     151   OCF.sub.3 H       3,3-diMe-1-Piz     152   OCF.sub.3 H       4-Me-1-Piz     153   OCF.sub.3 H       3,4-diMe-1-Piz     154   OCF.sub.3 H       4-Et-1-Piz     155   OCF.sub.3 H       4-(2-HOEt)-1-Piz     156   OCF.sub.3 H       4-(2-MeOEt)-1-Piz     157   OCF.sub.3 H       4-(2-AcOEt)-1-Piz     158   OCF.sub.3 H       4-(2-NH.sub.2 Et)-1-Piz     159   OCF.sub.3 H       4-(4-NH.sub.2 Bz)-1-Piz     160   OCF.sub.3 H       4-HCO-1-Piz     161   OCF.sub.3 H       4-Ac-1-Piz     162   OCF.sub.3 H       4-(AcMe)-1-Piz     163   OCF.sub.3 H       4-(HOOCMe)-1-Piz     164   OCF.sub.3 H       4-(EtcMe)-1-Piz     165   OCF.sub.3 H       1-Diz     166   OCF.sub.3 H       4-Me-1-Diz     167   OCF.sub.3 H       3-oxo-1-Piz     168   OCF.sub.3 H       4-Me-3-oxo-1-Piz     169   OCF.sub.3 H       3-HO-1-Azt     170   OCF.sub.3 H       3-HO-1-Pyrd     171   OCF.sub.3 H       3-HO-4-MeO-1-Pyrd     172   OCF.sub.3 H       3,4-diMeO-1-Pyrd     173   OCF.sub.3 H       3-NH.sub.2 -1-Azt     174   OCF.sub.3 H       3-NHMe-1-Azt     175   OCF.sub.3 H       3-NHEt-1-Azt     176   OCF.sub.3 H       3-(NH.sub.2 Me)-1-Azt     177   OCF.sub.3 H       3-[(NHMe)Me]-1-Azt     178   OCF.sub.3 H       3-[(NMe.sub.2)Me]-1-Azt     179   OCF.sub.3 H       3-NH.sub.2 -1-Pyrd     180   OCF.sub.3 H       3-NHMe-1-Pyrd     181   OCF.sub.3 H       3-NMe.sub.2 -1-Pyrd     182   OCF.sub.3 H       3-(NH.sub.2 Me)-1-Pyrd     183   OCF.sub.3 H       3-[(NHMe)Me]-1-Pyrd     184   OCF.sub.3 H       3-[(NHEt)Me]-1-Pyrd     185   OCF.sub.3 H       3-[(NMe.sub.2)Me]-1-Pyrd     186   OCF.sub.3 H       3-NH.sub.2 -4-Me-1-Pyrd     187   OCF.sub.3 H       3-NH.sub.2 -4-HO-1-Pyrd     188   OCF.sub.3 H       3-NH.sub.2 -4-MeO-1-Pyrd     189   OCF.sub.3 H       3-NH.sub.2 -4-EtO-1-Pyrd     190   OCF.sub.3 H       4-NH.sub.2 -1-Pip     191   OCF.sub.3 H       4-NHMe-1-Pip     192   OCF.sub.3 H       3-NH.sub.2 -1-Pip     193   OCF.sub.3 H       3-NHMe-1-Pip     194   OCF.sub.3 H       3-NMe.sub.2 -1-Pip     195   OCF.sub.3 H       3-NH.sub.2 -1-Azp     196   OCF.sub.3 H       3-NH.sub.2 -3-Me-1-Pyrd     197   OCF.sub.3 H       1-Imid     198   OCF.sub.3 H       4-Me-1-Imid     199   OCF.sub.3 H       Mor     200   OCF.sub.3 H       Thz     201   OCH.sub.2 F                     H       3,3-diMe-1-Piz     202   OCH.sub.2 F                     H       4-Me-1-Diz     203   OCH.sub.2 F                     H       1-Piz     204   OCH.sub.2 F                     H       1-Diz     205   OCH.sub.2 F                     H       3-NH.sub.2 -1-Pyrd     206   OCH.sub.2 F                     H       3-Me-1-Piz     207   OCH.sub.2 F                     H       4-Me-1-Piz     208   OCH.sub.2 F                     H       3-NH.sub.2 -4-Me-1-Pyrd     209   OCH.sub.2 F                     H       3,5-diMe-1-Piz     210   OCH.sub.2 F                     H       3,4-diMe-1-Piz     211   OCH.sub.2 F                     H       3-NHMe-1-Pyrd     212   OCH.sub.2 F                     H       3-NMe.sub.2 -1-Pyrd     213   OCF.sub.3 NH.sub.2                             1-Piz     214   OCF.sub.3 NH.sub.2                             3-Me-1-Piz     215   OCF.sub.3 NH.sub.2                             3,5-diMe-1-Piz     216   OCF.sub.3 NH.sub.2                             2,5-diMe-1-Piz     217   OCF.sub.3 NH.sub.2                             3,3-diMe-1-Piz-     218   OCF.sub.3 NH.sub.2                             4-Me-1-Piz     219   OCF.sub.3 NH.sub.2                             3,4-diMe-1-Piz     220   OCF.sub.3 NH.sub.2                             4-Et-1-Piz     221   OCF.sub.3 NH.sub.2                             4-(2-HOEt)-1-Piz     222   OCF.sub.3 NH.sub.2                             4-(2-MeOEt)-1-Piz     223   OCF.sub.3 NH.sub.2                             4-(2-AcOEt)-1-Piz     224   OCF.sub.3 NH.sub.2                             4-(2-NH.sub.2 Et)-1-Piz     225   OCF.sub.3 NH.sub.2                             4-(4-NH.sub.2 Bz)-1-Piz     226   OCF.sub.3 NH.sub.2                             4-HCO-1-Piz     227   OCF.sub.3 NH.sub.2                             4-Ac-1-Piz     228   OCF.sub.3 NH.sub.2                             4-(AcMe)-1-Piz     229   OCF.sub.3 NH.sub.2                             4-(HOOCMe)-1-Piz     230   OCF.sub.3 NH.sub.2                             4-(EtcMe)-1-Piz     231   OCF.sub.3 NH.sub.2                             1-Diz     232   OCF.sub.3 NH.sub.2                             4-Me-1-Diz     233   OCF.sub.3 NH.sub.2                             3-oxo-1-Piz     234   OCF.sub.3 NH.sub.2                             4-Me-3-oxo-1-Piz     235   OCF.sub.3 NH.sub.2                             3-HO-1-Azt     236   OCF.sub.3 NH.sub.2                             3-HO-1-Pyrd     237   OCF.sub.3 NH.sub.2                             3-HO-4-MeO-1-Pyrd     238   OCF.sub.3 NH.sub.2                             3,4-diMeO-1-Pyrd     239   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -1-Azt     240   OCF.sub.3 NH.sub.2                             3-NHMe-1-Azt     241   OCF.sub.3 NH.sub.2                             3-NHEt-1-Azt     242   OCF.sub.3 NH.sub.2                             3-[(NH.sub.2)Me]-1-Azt     243   OCF.sub.3 NH.sub.2                             3-(NHMeMe)-1-Azt     244   OCF.sub.3 NH.sub.2                             3-[(NMe.sub.2)Me]-1-Azt     245   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -1-Pyrd     246   OCF.sub.3 NH.sub.2                             3-NHMe-1-Pyrd     247   OCF.sub.3 NH.sub.2                             3-NMe.sub.2 -1-Pyrd     248   OCF.sub.3 NH.sub.2                             3-[(NH.sub.2)Me]-1-Pyrd     249   OCF.sub.3 NH.sub.2                             3-[(NHMe)Me]-1-Pyrd     250   OCF.sub.3 NH.sub.2                             3-[(NHEt)Me]-1-Pyrd     251   OCF.sub.3 NH.sub.2                             3-[(NMe.sub.2)Me]-1-Pyrd     252   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -4-Me-1-Pyrd     253   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -4-HO-1-Pyrd     254   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -4-MeO-1-Pyrd     255   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -4-EtO-1-Pyrd     256   OCF.sub.3 NH.sub.2                             4-NH.sub.2 -1-Pip     257   OCF.sub.3 NH.sub.2                             4-NHMe-1-Pip     258   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -1-Pip     259   OCF.sub.3 NH.sub.2                             3-NHMe-1-Pip     260   OCF.sub.3 NH.sub.2                             3-NMe.sub.2 -1-Pip     261   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -1-Azp     262   OCF.sub.3 NH.sub.2                             3-NH.sub.2 -3-Me-1-Pyrd     263   OCF.sub.3 NH.sub.2                             1-Imid     264   OCF.sub.3 NH.sub.2                             4-Me-1-Imid     265   OCF.sub.3 NH.sub.2                             Mor     266   OCF.sub.3 NH.sub.2                             Thz     267   OCH.sub.2 F                     NH.sub.2                             3,3-diMe-1-Piz     268   OCH.sub.2 F                     NH.sub.2                             4-Me-1-Diz     269   OCH.sub.2 F                     NH.sub.2                             1-Piz     270   OCH.sub.2 F                     NH.sub.2                             1-Diz     271   OCH.sub.2 F                     NH.sub.2                             3-NH.sub.2 -1-Pyrd     272   OCH.sub.2 F                     NH.sub.2                             3-Me-1-Piz     273   OCH.sub.2 F                     NH.sub.2                             4-Me-1-Piz     274   OCH.sub.2 F                     NH.sub.2                             3-NH.sub.2 -4-Me-1-Pyrd     275   OCH.sub.2 F                     NH.sub.2                             3,5-diMe-1-Piz     276   OCH.sub.2 F                     NH.sub.2                             3,4-diMe-1-Piz     277   OCH.sub.2 F                     NH.sub.2                             3-NHMe-1-Pyrd     278   OCH.sub.2 F                     NH.sub.2                             3-NMe.sub.2 -1-Pyrd     279   OCHF.sub.2                     H       3-(HOMe)-1-Piz     280   OCHF.sub.2                     NH.sub.2                             3-(HOMe)-1-Piz     281   OCHF.sub.2                     H       4-(SfoMe)-3-Me-1-Piz     282   OCHF.sub.2                     NH.sub.2                             4-(SfoMe)-3-Me-1-Piz     283   OCHF.sub.2                     H       4-(AcEt)-1-Piz     284   OCHF.sub.2                     NH.sub.2                             4-(AcEt)-1-Piz     285   OCHF.sub.2                     H       4-(AcEt)-3-Me-1-Piz     286   OCHF.sub.2                     NH.sub.2                             4-(AcEt)-3-Me-1-Piz     ______________________________________     Ac              acetyl     Azp             perhydroazepinyl     Azt             azetidinyl     Bz              benzyl     Diz             perhydro-1,4-diazepinyl                     (= homopiperazinyl)     Et              ethyl     Etc             ethoxycarbonyl     Imid            imidazolyl     Me              methyl     Mor             morpholino     Pip             piperidyl     Piz             piperazinyl     iPr             isopropyl     Pyrd            pyrrolidinyl     Sfo             sulfo     Thz             perhydro-1,4-thiazin-4-yl                     (= thiomorpholino)

Of the compounds listed above, the following are preferred, that is to say Compounds No. 1, 2, 3, 5, 24, 34, 39, 41, 43, 45, 46, 48, 56, 59, 72, 74, 75, 76, 78, 79, 82, 93, 94, 97, 107, 114, 116, 129, 131, 133, 136, 137, 139, 141, 142, 144, 179, 186, 202, 203, 204, 205, 206, 207, 208, 209, 213, 214, 245, 252, 268, 269, 270, 271, 272, 273, 274, 275, 279, 280, 281, 282, 283, 284, 285 and 286, and the following are the more preferred, that is to say Compounds No. 1, 2, 3, 5, 34, 39, 43, 45, 46, 48, 56, 59, 72, 74, 75, 76, 78, 79, 82, 93, 94, 107, 116, 129, 131, 133, 136, 137, 139, 141, 142, 144, 179 and 284.

The following are the most preferred:

1. 1-Cyclopropyl-8-difluoromethoxy-6-fluoro-7-(1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

2. 1-Cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

3. 1-Cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3,5-dimethyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

34. 1-Cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-amino-1-pyrrolidinyl) -1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

74. 5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

75. 5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

76. 5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3,5-dimethyl-1-piperazinyl)-l.4-dihydro-4-oxoquinoline-3-carboxylic acid;

78. 5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(4-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

93. 5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(1-homopiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

107. 5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-amino-1-pyrrolidinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

139. 5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro- 7-(3-fluoromethyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid;

144. 5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methyl-1-homopiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid.

Also preferred are pharmaceutically acceptable salts, esters and amides, more preferably salts and esters, and most preferably hydrochlorides and methanesulfonates, of the above preferred and most preferred Compounds.

In general terms, the compounds of the present invention may be prepared by reacting a compound of formula (VI): ##STR13## (in which R¹ and R³ are as defined above; X represents a halogen atom and is preferably a fluorine atom; and R¹³ represents a hydrogen atom or a carboxy-protecting group) or an active derivative or equivalent thereof with a compound of formula (VII):

    R.sup.2 --H                                                (VII)

(in which R² is as defined above) or an active derivative or equivalent thereof, and, if necessary, subjecting the product to any one or more of the reactions: deprotection, salification, esterification and amidation.

R¹³ may represent any carboxy-protecting group known in organic chemistry for use with this type of compound and may be incorporated into and (if desired) removed from the compound by well known methods which require no elaboration here. However, R¹³ is preferably a hydrogen atom or a C₁ -C₆, preferably C₁ -C₄, alkyl group, for example a methyl, ethyl, propyl, isopropyl, butyl, t-butyl, or hexyl group, most preferably a hydrogen atom, a methyl group or an ethyl group.

Alternatively, R¹³ may represent a boron difluoride (BF₂) group. In this case, the boron difluoride group will normally form a coordinate bond with the oxygen atom at the 4-position of the quinoline ring.

A preferred method of preparing the compounds of the invention is illustrated in more detail by Reaction Scheme A: ##STR14##

In the above formulae, R¹, R², R³, X and R¹³ are as defined above.

In the reactions shown in the above reaction scheme, the compounds of formula (I) of the present invention can be prepared by reacting a compound of formula (VI) or its boron difluoride chelate of formula (IX) with an amine compound of formula (VII) in Steps A1 and A3, respectively. The reaction may be effected in the presence or absence of an acid binding agent and in the presence or absence of a solvent.

The molar ratio of the compound of formula (VI) or (IX) to the amine of formula (VII) is not critical, although we generally prefer to employ equimolar amounts of the two reagents or a molar excess of the amine.

Where a solvent is employed, its nature is not particularly critical, provided that it has no adverse effect on the reaction. Examples of suitable solvents include: aprotic polar solvents, especially sulfoxides, such as dimethyl sulfoxide, or amides, such as dimethylformamide, hexamethylphosphoric triamide or dimethylacetamide; however, other solvents may also be used, including: ketones, such as acetone or methyl ethyl ketone; ethers, such as diethyl ether, tetrahydrofuran or dioxane; esters, such as ethyl acetate; alcohols, such as methanol, ethanol, propanol, isopropanol or butanol; and nitriles, such as acetonitrile. Of these, the aprotic polar solvents are preferred.

Where an acid binding agent is employed, its nature is likewise not particularly critical, provided that it has no adverse effect on the reaction and that it is capable of binding to, and hence effectively removing from the reaction, the acid produced in the course of the reaction. Examples of suitable acid binding agents include: tertiary amines, such as 1,8-diazabicyclo-[5.4.0]-7-undecene, 1,5-diazabicyclo[4.3.0]-5-nonene, triethylamine, tributylamine, pyridine, picoline, lutidine or collidine; and inorganic bases, preferably alkali metal carbonates, such as sodium carbonate or potassium carbonate, or alkali metal alkoxides, such as sodium methoxide, sodium ethoxide or potassium t-butoxide. The amount of acid binding agent employed is preferably equimolar or a molar excess, with respect to the compound of formula (VI) or (IX), more preferably a molar ratio of said compound of formula (VI) or (IX) to said acid binding agent of from 1:1 to 1:5. However, where one of the afore-mentioned amines is used as acid binding agent, it is preferably employed in a large excess, in which case it may serve both as the acid binding agent and as solvent. The reaction may also proceed smoothly even when an acid binding agent is not employed because an excess of the amine of formula (VII) can serve as the acid binding agent.

The reaction may be carried out over a wide range of temperatures, and the exact reaction temperature is not critical to the invention. However, we generally find it convenient to carry out the reaction at a temperature ranging from 0° C. to 200° C.

In the compound of formula (VIII) where R¹³ represents a carboxy-protecting group, this is then removed to prepare the corresponding compound where R¹³ represents a hydrogen atom. This removal may be effected by well known methods appropriate to the nature of the carboxy-protecting group represented by R¹³.

After the reaction is complete, the desired compound of the invention can be recovered from the reaction mixture by treatment in a conventional manner, and, if desired, may be further purified by such conventional techniques as recrystallization or the various chromatography techniques, notably column chromatography.

In the reactions represented by steps A2 to A6, a chelate of formula (X) of the desired compound is obtained first, and this is then converted into the BF₂ X addition product (XI) of the compound of formula (I) or the compound of formula (I) itself by treatment with an aqueous alcohol or a basic aqueous alcohol. The BF₂ X addition product (XI) of the compound of formula (I) is easily converted into the compound (I) itself by treatment with a base.

Examples of bases which may be employed include: alkali metal hydroxides, such as sodium hydroxide or potassium hydroxide; alkali metal carbonates, such as sodium carbonate or potassium carbonate; alkali metal alkoxides, such as sodium methoxide, sodium ethoxide or potassium t-butoxide; and tertiary amines, such as 1,8-diazabicyclo[5.4.0]-7-undecene, 1,5-diazabicyclo-[4.3.0]-5-nonene, triethylamine or 4-dimethylaminopyridine.

The compound of formula (I) or its BF₂ X addition product (XI) may, if desired, be converted into a desired salt by conventional means.

Conversion of the compound of formula (VI) to the boron difluoride chelate of formula (IX) can be carried out, for example, by reaction with hydrofluoroboric acid or boron trifluoride by the method described in Japanese Patent Application Kokai (i.e. as laid open to public inspection) No. 67290/84.

The compound of formula (I) thus prepared may exist as a mixture of optical isomers due to the presence of an asymmetric carbon atom in the moiety of the compound represented by R² or as geometric (cis or trans) isomers due to, for example, the presence of two or more substituents on the heterocyclic group represented by R². In such a case, individual isomers of the compound may be prepared, if desired, by using as the starting material of formula R² --H (VII) a compound which has been optically resolved or separated in advance to obtain the corresponding optical or geometric isomer of the desired compound (I). Alternatively, a mixture of optical or geometric isomers of the compound (I) may be prepared, and these may be resolved or separated into the individual isomers by conventional techniques.

The compounds of formula (VI) used as starting materials in the afore-mentioned reactions can be prepared, for instance, by the following Reaction Scheme B. ##STR15##

In the above formulae:

R¹, R³ and X are as defined above;

R^(3') represents hydrogen atom or a nitro (NO₂) group;

R¹⁷ represents a carboxy-protecting group, as illustrated in relation to the groups which may be represented by R¹³ ;

X' represents a halogen atom, such as a fluorine, chlorine, bromine or iodine group;

R¹⁴ and R¹⁵ are the same or different and each represents a C₁ -C₆ alkyl group, for example as exemplified above in relation to the alkyl groups which may be represented by R⁴, or R¹⁴ and R¹⁵ may, together with the nitrogen atom to which they are attached form a heterocyclic group having from 5 to 6 ring atoms of which 0 or 1 is an additional hetero-atom selected from the group consisting of nitrogen, oxygen and sulfur hereto-atoms and which is unsubstituted or as one or two oxo substituents on a sulfur hetero-atom to form a sulfinyl or sulfonyl group;

Ac represents the acetyl group;

Et represents the ethyl group; and

Ts represents the p-tosyl (p-toluenesulfonyl) group.

The reaction conditions and treatment after completion of the reaction in each Step are described in more detail in the following Preparations. Of course, the details of reaction conditions etc given in these Preparations are merely by way of example and it will be appreciated that these well known reactions may be conducted in a variety of different ways.

In Step B8, examples of suitable bases include: alkali metal hydrides, such as sodium hydride or potassium hydride; alkali metal carbonates, such as sodium carbonate or potassium carbonate; and alkali metal alkoxides, such as sodium methoxide or potassium t-butoxide.

In the compound of formula (XX), where R^(3') represents a hydrogen atom, the compound may be the desired compound of formula (VI) or it may be hydrolised in Step B9 to give the free acid of formula (XXI). However, where R^(3') represents a nitro group, it is necessary that this should be reduced to an amino group and form the compound of formula (XXII); this may be the desired compound or it may likewise be hydrolised to give the compound of formula (XXI).

Where R^(3') in the compound of formula (XII) used as the starting material in this Reaction Scheme represents a nitro group, this compound may be prepared by nitration of the corresponding Compound where R^(3') represents a hydrogen atom, e.g. as shown below: ##STR16##

As an alternative to Steps B8, B10 and B11, where R^(3') represents a nitro group, the compound of formula (XIX) [shown in the following Scheme as formula (XIXa)] may be reduced to give the amino compound; also the compound of formula (XVIII) where R^(3') represents a nitro group [shown in the following Scheme as formula (XVIIIa)] may be reduced to the corresponding amino compound; after which the products may be treated as shown also in Reaction Scheme B': ##STR17##

In the above formulae, R¹, R¹⁴, R¹⁵, R¹⁷, X and X' are as defined above.

Those compounds of formula (XII) in which R^(3') represents a hydrogen atom and R¹ represents a difluoromethoxy group can be prepared as shown in Reaction Scheme C, whilst those in which R^(3') represents a hydrogen atom and R¹ represents a trifluoromethoxy group can be prepared as shown in Reaction Scheme D: ##STR18##

In the above formulae, X and X' are as defined above, R¹⁶ represents a C₁ -C₆ alkoxy group or an amino group; and X^(a) and X^(b) are the same or different and each represents a halogen atom, for example a chlorine, bromine or iodine atom, but not a fluorine atom.

In Reaction Scheme C, by replacing the compound of formula X^(a) --CHF₂ by a compound of formula X^(a) --CHF₂, the corresponding compounds having a monofluoromethoxy group at the 3-position can be prepared.

2,4,5-Trifluoro-3-hydroxybenzoic acid, and the corresponding compounds having other halogen atoms at the 2- and 4- positions, which may be employed as the starting materials in these Reaction Schemes, can be prepared by the decarboxylation by heating of the known compound, 3,5,6-trifluoro-4-hydroxyphthalic acid, or the corresponding compounds having other halogen atoms at the 3- and 5- positions, in an aqueous medium, e.g. water or an aqueous solvent, as shown below: ##STR19##

The compounds of the invention possess a powerful antibacterial activity. Estimation by the agar plate dilution method showed an excellent growth inhibitory effect against a wide range of pathogenic bacteria, including Gram-positive bacteria such as Staphylococcus aureus or Enterococcus species, and Gram-negative bacteria such as Escherichia coli, dysentery bacillus, Shigella, Klebsiella pneumoniae, Myxomycetes, Serratia, Enterobacter, Salmonella or Pseudomonas aeruginosa, including normally resistant strains thereof.

The compounds of the invention can be administered as conventional pharmaceutical formulations, depending upon the intended route of administration. For example, for oral administration, they may be formulated as powders, granules, tablets, capsules, syrups or similar orally administerable formulations, which can be produced by mixing the active compound with carriers, excipients or diluting agents, such as glucose, sucrose, lactose, sorbitol, starch, polyvinylpyrrolidone, mannitol, calcium carbonate, calcium phosphate, sodium chloride or boric acid. For parenteral administration, they may be formulated as conventional injections suitable for, for example, intravenous or intramuscular injection. The dose will vary, depending upon the nature of the disorder, the route of administration, and the symptoms, age and body weight of the patient; however, for an adult human patient, a suitable dose for oral administration would be from 100 mg to 1000 mg per day, which could be given in a single dose or in divided doses.

The invention is further illustrated by the following Examples, which illustrate the preparation of various of the compounds of the invention. The preparation of certain of the starting materials employed in these Examples is illustrated in the Preparations. The activity of certain of the compounds of the invention is illustrated by the subsequent Biological Activity data.

PREPARATION 1

3-Difluoromethoxy-2,4,5-trifluorobenzoic acid [(XXV), X=X'=F] (ester route)

1(a) Ethyl 2,4,5-trifluoro-3-hydroxybenzoate [(XXIV), X=X'=F, R¹⁶ =C₂ H-₅ O]

5 ml of concentrated sulfuric acid were added to a solution of 20.0 g (0.104 moles) of 2,4,5-trifluoro-3-hydroxybenzoic acid [(XXIII), X=X'=F] (prepared as described in Preparation 13) in 500 ml of ethanol, and the mixture was heated under reflux for 4 hours. The ethanol was then removed by distillation under reduced pressure, and the residue was extracted with ethyl acetate. The extract was washed with a saturated aqueous solution of sodium bicarbonate and with water, in that order, after which it was dried over anhydrous sodium sulfate and then concentrated by evaporation under reduced pressure, to give 16.9 g of ethyl 2,4,5-trifluoro-3-hydroxybenzoate as a colorless powder.

Mass Spectrum (CI): m/e 221 (M⁺ +1), 175 (M⁺ --OC₂ H₅)

("CI" means "chemical ionization").

1(b) Ethyl 3-difluoromethoxy-2,4,5-trifluorobenzoate [(XXVI), X=X'=F, R¹⁶ =C₂ H₅ O]

1.76 g (0.044 moles) of a 60% w/w suspension of sodium hydride in mineral oil was added in small portions, whilst stirring and ice-cooling, to a solution of 8.83 g (0.04 moles) of ethyl 2,4,5-trifluoro-3-hydroxybenzoate [(XXIV), X=X'=F, R¹⁶ =C₂ H₅ O] [prepared as described in step (a) above] in 40 ml of dimethylformamide and, after the addition was complete, the mixture was stirred, whilst ice-cooling, for an additional 30 minutes. At the end of this time, the reaction mixture was transferred into a 200 ml stainless steel autoclave, and then 100 ml of dimethylformamide containing 28.0 g (0.32 moles) of chlorodifluoromethane were added thereto, and the mixture was stirred under pressure at 95°-100° C. for 5 hours. At the end of this time, the dimethylformamide was removed by distillation under reduced pressure, and water was added to the residue, which was extracted with toluene. The extract was washed with water and dried over anhydrous sodium sulfate, and then the solvent was removed by evaporation under reduced pressure. The residue was subjected to silica gel column chromatography, using toluene as the eluent, to give 4.85 g of ethyl 3-difluoromethoxy-2,4,5-trifluorobenzoate as a colorless liquid.

Mass Spectrum (CI): m/e 271 (M⁺ +1), 225 (M⁺ --OC₂ H₅).

1(c) 3-Difluoromethoxy-2,4,5-trifluorobenzoic acid [(XXV), X=X'=F]

20 ml of a 6% w/v aqueous solution of sodium hydroxide were added to a solution of 5.79 g (0.021 moles) of ethyl 3-difluoromethoxy-2,4,5-trifluorobenzoate [(XXVI), X=X'=F, R¹⁶ =C₂ H₅ O] [prepared as described in step (b) above] in 40 ml of ethanol, and the mixture was left at room temperature overnight. The reaction mixture was then acidified by the addition of 3.5 ml of concentrated aqueous hydrochloric acid, and, after concentration by evaporation under reduced pressure, it was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous sodium sulfate, and then the solvent was removed by distillation under reduced pressure, to give 5.22 g of 3-difluoromethoxy-2,4,5-trifluorobenzoic acid as a colorless powder, melting at 68°-70° C.

Mass Spectrum (CI): m/e 243 (M⁺ +1), 225 (M⁺ --OH), 223 (M⁺ --F), 192 (M⁺ --CF₂), 175 (M⁺ --CF₂ --OH).

Nuclear Magnetic Resonance Spectrum (CDCl₃, δ ppm): 6.67 (1H, triplet, J=72 Hz); 7.83 (1H, multiplet); 10.74 (1H, broad).

PREPARATION 2

3-Difluoromethoxy-2,4,5-trifluorobenzoic acid [(XXV), X=X'=F] (amide route)

2(a) 2,4,5-Trifluoro-3-hydroxybenzoyl amide [(XXIV), X=X'=F, R¹⁶ =NH₂ ]

300 ml of thionyl chloride were added to a solution of 100.0 g (0.52 moles) of 2,4,5-trifluoro-3-hydroxybenzoic acid [(XXIII), X=X'=F] (prepared as described in Preparation 13) in 400 ml of benzene, and the mixture was heated under reflux for 3 hours. At the end of this time, the solvent and excess thionyl chloride were removed by distillation under reduced pressure, to give 2,4,5-trifluoro-3-hydroxybenzoyl chloride. The whole of this chloride was added dropwise to 1500 ml of 28% w/v aqueous ammonia, whilst stirring and ice-cooling, and the mixture was then stirred for a further 2 hours. At the end of this time, the mixture was allowed to stand at room temperature overnight, after which it was acidified by the addition of dilute aqueous hydrochloric acid. The reaction mixture was then extracted with ethyl acetate, and the extract was washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, to give 88.2 g of 2,4,5-trifluoro-3-hydroxybenzoyl amide as a colorless powder, melting at 153°-155° C.

Mass Spectrum (CI): m/e 192 (M⁺ +1), 175 (M⁺ --NH2).

2(b) 3-Difluoromethoxy-2,4,5-trifluorobenzoyl amide [(XXVI), X=X'=F, R¹⁶ =NH₂ ]

5.00 g (0.026 moles) of 2,4,5-trifluoro-3-hydroxybenzoyl amide [(XXIV), X=X'=F, R¹⁶ =NH₂ ][prepared as described in step (a) above] were dissolved in 130 ml of dimethylformamide. 4.70 g (0.034 moles) of potassium carbonate and 6.8 g (0.079 moles) of chlorodifluoromethane were then added to the resulting solution, and the mixture was stirred in an autoclave at 100° C. for 3 hours. At the end of this time, 500 ml of water were added to the reaction mixture, which was then extracted with ethyl acetate. The extract was washed with water, and the solvent was removed by evaporation under reduced pressure. The residue was subjected to silica gel column chromatography, using a 1:1 by volume mixture of toluene and ethyl acetate as the eluent, to give 5.08 g of 3-difluoromethoxy-2,4,5-trifluorobenzoyl amide as colorless needles, melting at 102°-104° C.

Mass Spectrum (CI): m/e 242 (M⁺ +1), 225 (M⁺ --NH₂).

2(c) 3-Difluoromethoxy-2,4,5-trifluorobenzoic acid [(XXV), X=X'=F]

30 ml of an aqueous solution containing 6.60 g (0.096 moles) of sodium nitrite were slowly added dropwise, whilst stirring and ice-cooling, to a suspension of 15.53 g (0.064 moles) of 3-difluoromethoxy-2,4,5-trifluorobenzoyl amide [(XXVI), X=X'F, R¹⁶ --NH₂ ] [prepared as described in step (b) above] in 20 ml of concentrated aqueous sulfuric acid, and the mixture was heated under reflux for 30 minutes. At the end of this time, it was cooled to room temperature, and then 50 ml of water were added it. The reaction mixture was then extracted with chloroform. The extract was washed with water and dried over anhydrous sodium sulfate, and then the solvent was removed by distillation under reduced pressure, to give 15.59 g of 3-difluoromethoxy-2,4,5-trifluorobenzoic acid as a colorless powder.

This compound had the same melting point, mass spectrum and nuclear magnetic resonance spectrum data as that obtained through the ester route in Preparation 1.

PREPARATION 3

3-Difluoromethoxy-2,4,5-trifluorobenzoic acid [(XXV), X=X'=F] (direct method)

20 ml of dimethylformamide, followed by 4.97 g (0.026 mole) of 2.4,5-trifluoro-3-hydroxybenzoic acid [(XXIII), X=X'=F], were added in portions, whilst ice-cooling, to a solution of 2.18 g (0.052 mole) of sodium hydroxide in 5 ml of water. Thereafter the solution was stirred for 30 minutes, whilst ice-cooling. The reaction mixture was then transferred to a 200 ml stainless steel autoclave, and 100 ml of dimethylformamide containing 24.0 g (0.277 mole) of chlorodifluoromethane were added to it. The mixture was then stirred at between 100° and 110° C. for 5 hours under pressure. At the end of this time, the reaction mixture was poured into water and extracted with chloroform. The chloroform extracts were washed with water and dried over anhydrous sodium sulfate; the solvent was then removed by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 9:1 by volume mixture of ethyl acetate and ethanol as the eluent, to afford 2.00 g of 3-difluoromethoxy-2,4,5-trifluorobenzoic acid as a colorless powder.

This compound had the same melting point, mass spectrum and nuclear magnetic resonance spectrum data as that obtained through the ester route in Preparation 1.

PREPARATION 4

2,4,5-Trifluoro-3-trifluoromethoxybenzoic acid [(XXIX), X=X'=F]

4(a) Ethyl 3-bromodifluoromethoxy-2,4,5-trifluorobenzoate [(XXVII), X=X'=F, X^(a) =Br, R¹⁶ =C₂ H₅ O]

1.0 g (0.025 moles) of a 60% w/w suspension of sodium hydride in mineral oil was added in small portions, whilst stirring and ice-cooling, to a solution of 5.0 g (0.023 moles) of ethyl 2,4,5-trifluoro-3-hydroxybenzoate [(XXIV), X=X'=F, R¹⁶ =C₂ H₅ O ] [prepared as described in Preparation 1(a)] in 20 ml of dimethylformamide and, after completion of the addition, the mixture was stirred, whilst ice-cooling, for an additional 30 minutes. After this, 30 ml of dimethylformamide containing 28.0 g (0.13 moles) of dibromodifluoromethane were added, and the mixture was stirred at room temperature for 23 hours. At the end of this time, the reaction mixture was poured into 300 ml of water, and extracted with toluene. The extract was washed with water and dried over anhydrous sodium sulfate, and then the solvent was removed by distillation under reduced pressure. The residue was subjected to silica gel column chromatography, using toluene as the eluent, to give 5.60 g of ethyl 3-bromodifluoromethoxy-2.4,5-trifluorobenzoate as a colorless liquid.

Mass Spectrum (CI): m/e 351 (M⁺ +3), 349, (M⁺ +1).

4(b) Ethyl 2,4,5-trifluoro-3-trifluoromethoxybenzoate [(XXVIII), X=X'=F, R¹⁶ =C₂ H₅ O]

1.50 g (0.0043 moles) of ethyl 3-bromodifluoromethoxy-2,4,5-trifluorobenzoate [(XXVII), X=X'=F, X^(a) =Br, R¹⁶ =C₂ H₅ O] [prepared as described in step (a) above] was dissolved in 10 ml of toluene, and 2.50 g (0.013 moles) of silver tetrafluoroborate were added thereto. The mixture was then heated under reflux for 8 hours in the dark, whilst stirring. At the end of this time, the reaction mixture was filtered, and the filtrate was washed with water, dried over anhydrous sodium sulfate, and concentrated by evaporation under reduced pressure. The residue was subjected to silica gel column chromatography, using toluene as the eluent, to give 1.12 g of ethyl 2,4,5-trifluoro-3-trifluoromethoxybenzoate as a colorless liquid.

Mass Spectrum (CI): m/e 289 (M⁺ +1), 269 (M⁺ --F).

4(c) 2,4,5-Trifluoro-3-trifluoromethoxybenzoic acid [(XXIX), X=X'=F]

19.3 ml (0.0193 moles) of a 1N aqueous solution of sodium hydroxide were added t9 a solution of 5.05 g (0.0175 moles) of ethyl 2,4,5-trifluoro-3-trifluoromethoxybenzoate [(XXVIII), X=X'=F, R¹⁶ =C₂ H₅ O] [prepared as described in step (b) above] in 100 ml of ethanol, and the mixture was allowed to stand at room temperature for 2 hours. At the end of this time, 19.3 ml of 1N aqueous hydrochloric acid were added, and then the reaction mixture was concentrated by evaporation under reduced pressure. The residue was then extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate, and evaporated to dryness under reduced pressure, to give 3.98 g of 2,4,5-trifluoro-3-trifluoromethoxybenzoic acid as a colorless powder.

Mass Spectrum (CI): m/e 261 (M⁺ +1), 243 (M⁺ --OH).

Nuclear Magnetic Resonance Spectrum (CDCl₃, δ ppm): 7.88 (1H, multiplier).

PREPARATION 5

3-Difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoic acid [(XII), R¹ =--OCHF₂, R^(3') =NO₂, X=X'=F]

20 ml of concentrated aqueous nitric acid (d=1.42) were added dropwise, whilst stirring and cooling with water, to a solution of 15.0 g (0.062 moles) of 3-difluoromethoxy-2,4,5-trifluorobenzoic acid [(XXV), X=X'=F] (prepared as described in Preparation 1, 2 or 3) in 40 ml of concentrated aqueous sulfuric acid, and the mixture was stirred at 60° C. for 7 hours. At the end of this time, it was allowed to stand to cool to room temperature, and then the reaction mixture was poured into ice-water, and extracted with diethyl ether. The extract was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous sodium sulfate; the solvent was then removed by evaporation under reduced pressure, to give 16.6 g of 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoic acid as a yellow powder, melting at 77°-80° C.

Mass Spectrum: m/e 287 (M⁺), 243 (M⁺ --CO₂).

PREPARATION 6

Ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XX), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =C₂ H₅, X=F]

6(a) Diethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylmalonate [(XIV), R¹ =--OCHF₂, =R^(3') =H, R¹⁷ =C₂ H₅, X=X'=F]

15 ml of thionyl chloride were added to a solution of 5.22 g (0.0216 moles) of 3-difluoromethoxy-2,4,5-trifluorobenzoic acid [(XII), R¹ --OCHF₂, R^(3') =H, X=X'=F] (prepared as described in Preparation 1, 2 or 3) in 300 ml of benzene, and the mixture was heated under reflux for 3 hours. At the end of this time, benzene and excess thionyl chloride were removed by distillation under reduced pressure, to give 3-difluoromethoxy-2,4,5-trifluorobenzoyl chloride [(XIII), R¹ =--OCHF₂, R^(3') =H, X=X'=F].

Meanwhile, a suspension of diethyl ethoxymagnesium malonate in diethyl ether was prepared from a mixture of 2.80 g (0.0238 moles) of magnesium ethoxide and 3.81 g (0.0238 moles) of diethyl malonate in 60 ml of anhydrous diethyl ether by heating under reflux for 1 hour, whilst stirring. A solution of the 3-difluoromethoxy-2,4,5-trifluorobenzoyl chloride prepared as described above in 50 ml of anhydrous diethyl ether was then added dropwise to the suspension, whilst stirring at room temperature, and the mixture was then stirred at room temperature for an additional 2 hours. 35 ml of 1N aqueous hydrochloric acid were added to the reaction mixture, and the mixture was vigorously stirred. The organic layer was then separated, washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure to give 7.07 g of diethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylmalonate [(XIV), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =C₂ H₅, X=X'=F] as a brown liquid.

Mass Spectrum (CI): m/e 385 (M⁺ +1), 339 (M⁺ --OC₂ H₅).

6(b) Ethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylacetate [(XV), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =C₂ H₅, X=X'=F].

The whole of the diethyl-3-difluoromethoxy-2,4,5trifluorobenzoylmalonate [(XIV), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =C₂ H₅, X=X'=F] [prepared as described in step (a) above] was dissolved in 200 ml of dioxane, and then 4.52 g (0.0238 moles) of p-toluenesulfonic acid monohydrate were added to the resulting solution. The mixture was then heated under reflux for 6 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure. 100 ml of water and 2.52 g (0.03 moles) of sodium bicarbonate were added to the residue, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous sodium sulfate, and the solvent was removed by distillation under reduced pressure to give 5.66 g of ethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylacetate as a reddish brown liquid.

Mass Spectrum (CI): m/e 313 (M⁺ +1), 225 (M⁺ --CH₂ COOC₂ H₅).

6(c) Ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluorobenzoyl)acrylate [(XIX), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =, C₂ H₅, X=X'=F]

20 ml of acetic anhydride and 6 ml of ethyl orthoformate were added to the whole of the ethyl 3-difluoromethoxy-2,4,5-trifluorobenzoylacetate [(XV), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =C₂ H₅, X=X'=F] prepared as described in step (b) above, and, after the mixture had been heated under reflux for 2 hours, the excess acetic anhydride and ethyl orthoformate were removed by evaporation under reduced pressure. The residue was dissolved in 200 ml of methylene chloride, and 1.25 g (0.022 moles) of cyclopropylamine was added dropwise, whilst stirring and ice-cooling; the stirring was continued, whilst ice-cooling, for an additional 1 hour. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, and the residue was subjected to silica gel column chromatography, using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to give 3.29 g of ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5trifluorobenzoyl)acrylate as an amber colored liquid.

Mass Spectrum (CI): m/e 380 (M⁺ +1), 225 [M⁺ --cPr--NH--CH═C(COOEt)].

6(d) Ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XX), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =C₂ H₅, X=F ]

The whole of the ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluorobenzoyl)acrylate [(XIX), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =C₂ H₅, X =X'=F] [prepared as described in step (c) above] was dissolved in 150 ml of anhydrous diethyl ether, and then 0.39 g (0.0098 moles) of a 60% w/w suspension of sodium hydride in mineral oil was added in portions, whilst stirring at room temperature to the resulting solution. After completion of the addition, the stirring was continued at room temperature for an additional 1 hour, and then the mixture was acidified by the addition of 1N aqueous hydrochloric acid with vigorous stirring. The reaction mixture was filtered and washed with water and with diethyl ether, in that order, to give 1.44 g of ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate as colorless needles, melting at 224°-226° C.

Mass Spectrum (CI): m/e 360 (M⁺ +1).

PREPARATION 7

1-Cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid [(XXI), R¹ =--OCHF₂, R³ =H, X=F]

9 ml of acetic acid, 1.2 ml of concentrated sulfuric acid and 7 ml of water were added to 1.40 g (0.0039 moles) of ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XX), R¹ =--OCHF₂, R^(3') =H, R¹⁷ =, C₂ H₅, X=F] (prepared as described in Preparation 6), and the mixture was heated under reflux for 1 hour. At the end of this time, it was cooled to room temperature and poured into ice-water. The precipitated crystals were collected by filtration and washed with water and with diethyl ether, in that order, to give 1.09 g of 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid as colorless needles, melting at 202°-207° C.

Mass Spectrum (CI): m/e 332 (M⁺ +1).

Elemental analysis: Calculated for C₁₄ H₉ F₄ NO₄ : C, 50.77%; H, 2.74%; N, 4.23%. Found: C, 50.53%; H; 2.79%; N, 4.06%.

PREPARATION 8

1-Cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid boron difluoride chelate [(IX), R¹ =--OCHF₂, R^(3'=) H, X=F]

5.63 g of boron trifluoride diethyl etherate were added to a solution of 9.50 g (0.0265 moles) of ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(VI), R¹ =--OCHF₂, R³ =H, R¹³ =C₂ H₅, X=F] (prepared as described in Preparation 6) in 150 ml of methyl isobutyl ketone, and the mixture was heated under reflux for 6 hours. At the end of this time, the reaction mixture was cooled with ice, and the precipitated crystals were collected by filtration and washed with diethyl ether and with chloroform, in that order, to give 6.15 g of 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid boron difluoride chelate as a colorless powder, melting at 225°-233° C.

Mass Spectrum (CI): m/e 380 (M⁺ +1).

Elemental analysis: Calculated for C₁₄ H₈ BF₆ NO₄.1/2H₂ O: C, 43.33%; H, 2.34%; N, 3.61%. Found: C, 43.06%; H, 2.09%; N, 3.78%.

PREPARATION 9

Ethyl 1-cyclopropyl-6,7-difluoro-8-trifluoromethoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate [(VI), R¹ =--OCF₃, R³ =H, R¹³ =C₂ H₅, X=F]

Following a procedure similar to that described in Preparation 6, but using 6.02 g of 2,4,5-trifluoro-3-trifluoromethoxybenzoic acid (prepared as described in Preparation 4) [(XXIX), X=X'=F], 2.41 g of ethyl 1-cyclopropyl-6,7-difluoro-8-trifluoromethoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate were obtained as colorless needles, melting at 160°-161° C.

Mass Spectrum (CI): m/e 378 (M⁺ +1).

PREPARATION 10

1-Cyclopropyl-6,7-difluoro-8-trifluoromethoxy-1,4-dihydro-4-oxoquinoline-3-carboxylic acid boron difluoride chelate [(IX), R¹ =--OCF₃, R³ =H, X=F]

Following a procedure similar to that described in Preparation 8, but using 2.10 g of ethyl 1-cyclopropyl -6,7-difluoro-8-trifluoromethoxy-1,4-dihydro-4-oxoquinoline-3-carboxylate [(VI), R¹ =--OCF₃, R³ =H, R¹³ =C₂ H₅, X=F] (prepared as described in Preparation 9), 1.82 g of 1-cyclopropyl-6,7-difluoro-8-trifluoromethoxy-1,4-dihydro-4-oxoquinoline-3-carboxylic acid boron difluoride chelate were prepared as a colorless powder, melting at 266°-271° C.

Mass Spectrum (CI): m/e 398 (M⁺ +1).

Elemental analysis:

Calculated for C₁₄ H₇ BF₇ NO₄.1/2H₂ O: C, 41.42% H; 1.99%; N, 3.45%. Found: C, 41.26%; H, 1.69%; N, 3.57%.

PREPARATION 11

5-Amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline 3-carboxylic acid [(XXII), R¹ =--OCHF₂, R¹⁷ =H, X=F]

11(a) Diethyl (3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl )malonate [(XIV), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=X'=F]

40 ml of thionyl chloride were added to a solution of 15.97 g (0.056 moles) of 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoic acid [(XII), R¹ =--OCHF₂, R^(3') =NO₂, X=X'=F] in 50 ml of benzene, and the mixture was heated under reflux for 2 hours. At the end of this time, the benzene and the excess thionyl chloride were removed by distillation under reduced pressure to give 16.50 g of 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl chloride [(XIII), R¹ =--OCHF₂, R^(3') =NO₂, X=X'=F].

Meanwhile, a suspension of diethyl ethoxymagnesium malonate in diethyl ether was prepared from a mixture of 6.82 g (0.058 moles) of magnesium ethoxide and 9.35 g (0.058 moles) of diethyl malonate in 150 ml of anhydrous diethyl ether by heating under reflux for 2 hours, whilst stirring.

The whole of the 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl chloride [(XIII), R¹ =--OCHF₂, R^(3') =NO₂, X=X'=F] prepared as described above was dissolved in 150 ml of anhydrous diethyl ether, and this solution was added dropwise, with stirring at room temperature, to the suspension of diethyl ethoxymagnesium malonate. The resulting mixture was then stirred at room temperature for an additional 2 hours. At the end of this time, 100 ml of 1N aqueous hydrochloric acid were added to the reaction mixture, and, after the mixture had been vigorously stirred, the organic layer was separated, washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by evaporation under reduced pressure to give 31.2 g of diethyl (3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)malonate [(XIV), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=X'=F] as a red liquid.

Mass Spectrum (CI): m/e 430 (M⁺ +1), 384 (M⁺ --OEt), 270 [M⁺ --CH(COOEt)₂ ].

11(b) Ethyl 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoylacetate [(XV), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=X'=F]

The whole of the diethyl (3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)malonate [(XIV), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=X'=F] obtained as described in step (a) above was dissolved in 300 ml of dioxane, and 10.6 g (0.056 moles) of p-toluenesulfonic acid monohydrate were added to the resulting solution. The mixture was then heated under reflux for 4 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure. 150 ml of water and 4.7 g (0.056 moles) of sodium bicarbonate were added to the residue, which was then extracted with toluene. The extract was washed With water and dried over anhydrous sodium sulfate; the solvent was then removed by distillation under reduced pressure, to give 19.4 g of ethyl 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoylacetate as a red liquid.

Mass Spectrum (CI): m/e 358 (M⁺ +1), 312 (M⁺ --OEt), 270 (M⁺ --CH₂ CO₂ Et).

11(c) Ethyl 2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)-3-ethoxyacrylate [(XVI), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅ X=X'=F]

38 ml of acetic anhydride and 11 ml of ethyl orthoformate were added to the whole of the ethyl 3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoylacetate [(XV), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=X'=F] prepared as described in step (b) above, and then the mixture was heated under reflux for 3 hours; the excess acetic anhydride and ethyl orthoformate were then removed by evaporation under reduced pressure, to give 20.6 g of ethyl 2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)-3-ethoxyacrylate as a red liquid.

Mass Spectrum (CI): m/e 414 (M⁺ +1), 367 (M⁺ --NO₂).

11(d) Ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)acrylate [(XIX), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅ X=X'=F]

The whole of the ethyl 2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)-3-ethoxyacrylate [(XVI), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=X'=F] obtained as described in step (c) above was dissolved in 500 ml of methylene chloride, and 3.5 g (0.06 moles) of cyclopropylamine were added dropwise to the resulting solution, whilst stirring and ice-cooling. The mixture was then stirred for 1 hour, whilst ice-cooling, and then for an additional 1 hour at room temperature, after which the solvent was removed by evaporation under reduced pressure. The resulting residue was subjected to silica gel column chromatography using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to give 19.8 g of ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)acrylate as an yellow powder, melting at 105°-106° C.

Mass Spectrum (CI): m/e 425 (M⁺ +1), 379 (M⁺ --OEt). 11(e) Ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-5-nitro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XX), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=F]

1.0 g (0.0024 moles) of ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluoro-8-nitrobenzoyl)acrylate [(XIX), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=X'=F] [prepared as described in step (d) above] was dissolved in 10 ml of tetrahydrofuran, and 0.094 g (0.0024 moles) of a 60% w/w suspension of sodium hydride in mineral oil was added to the resulting mixture. The mixture was then stirred at room temperature for 1 hour, after which 1N aqueous hydrochloric acid was added, and the mixture was vigorously stirred to acidify the whole mixture. The crystals which precipitated were collected by filtration and washed with water and with diethyl ether, in that order, to give 0.6 g of ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-5-nitro-1,4-dihydro-4-oxo-quinoline-3-carboxylate as a pale yellow powder, melting at 262°-268° C.

Mass Spectrum (CI): m/e 405 (M⁺ +1), 358 (M⁺ --NO₂).

Nuclear Magnetic Resonance Spectrum (hexadeuterated dimethyl sulfoxide, δ ppm): 1.05 (4H, multiplier); 1.22 (3H, triplet); 3.91 (1H, multiplier); 4.18 (2H, quartet); 7.24 (1H, triplet, J=72 Hz) 8.56 (1H, singlet).

11(f) Ethyl 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XXII), R¹ =--OCHF₂, R¹⁷ =C₂ H₅, X=F]

3.0 g (0.0074 moles) of ethyl 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-5-nitro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XX), R¹ =--OCHF₂, R^(3') =NO₂, R¹⁷ =C₂ H₅, X=F] [prepared as described in step (e) above] were dissolved in 800 ml of acetic acid by heating. 0.75 g of 5% w/w palladium-on-carbon was then added to the solution, and the mixture was stirred at 70°-80° C. for 3 hours under a current of hydrogen. At the end of this time, the reaction mixture was filtered, and the filtrate was concentrated by evaporation under reduced pressure. The residue was washed with diethyl ether to give 1.78 g of ethyl 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate as a colorless powder, melting at 295°-296° C.

Mass Spectrum (CI): m/e 375 (M⁺ +1), 329 (M⁺ --OEt).

11(f') Ethyl 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XXII), R¹ =--OCHF₂, R¹⁷ =C₂ H₅, X=F]

The compound of Preparation 11(f) was also synthesised by the following method.

33.63 g (0.079 mole) of ethyl 3-cyclopropylamino-2-(3-difluoromethoxy-2,4,5-trifluoro-6-nitrobenzoyl)acrylate [(XIXa): X=X'=F, R¹ =OCHF₂, R¹⁷ =C₂ H₅ ] were dissolved in 1300 ml of ethanol with heating. A stream of hydrogen was then bubbled through the solution in the presence of 8.4 g of 5% palladium-on-carbon at room temperature for 40 minutes, whilst stirring. At the end of this time, the reaction mixture was filtered, and the filtrate was concentrated by evaporation under reduced pressure. The resulting residue was then purified by silica gel column chromatography using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to give 25.1 g of ethyl 3-cyclopropylamino-2-(6-amino-3-difluoromethoxy-2,4,5-trifluorobenzoyl)acrylate [(XIXb): X=X'=F, R¹ =OCHF₂, R¹⁷ =C₂ H₅ ] as a pale yellow powder, melting at 103°-104° C.

Mass Spectrum (CI): m/e 395 (M⁺ +1).

The whole of the ethyl 3-cyclopropylamino-2-(6-amino-3-difluoromethoxy-2,4,5-trifluorobenzoyl)acrylate prepared as described above was dissolved in 340 ml of tetrahydrofuran, and 3.82 g (0.096 mole) of a 60% w/w dispersion of sodium hydride in mineral oil were added slowly to the resulting solution, whilst ice-cooling. The mixture was then stirred at the same temperature for 30 minutes, and then at room temperature for a further 1 hour. At the end of this time, the reaction mixture was acidified by the addition of 96 ml of 1N aqueous hydrochloric acid, whilst stirring vigorously. The resulting precipitate was collected by filtration and washed with water and with ethanol, in that order, to give 18.76 g of ethyl 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XXII), R¹ =--OCHF₂, R¹⁷ =C₂ H₅, X=F] as a colorless powder, melting at 295°-296° C.

Mass Spectrum (CI): m/e 375 (M⁺ +1).

11(g) 5-Amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid [(XXI) R¹ =--OCHF₂, R³ =NH₂, X=F]

A suspension of 3.58 g (0.0096 moles) of ethyl 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XXII), R¹ =--OCHF₂, R¹⁷ =C₂ H₅, X=F] [prepared as described in step (f) or (f') above], 21 ml of acetic acid, 2.8 ml of concentrated sulfuric acid and 15 ml of water was heated under reflux, with stirring, for 1 hour, after which it was cooled by allowing it to stand. Water was then added to the reaction mixture, and the insoluble materials were removed by filtration and washed with water and with diethyl ether, in that order, to give 3.0 g of 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid as a pale yellowish green powder, melting at 284°-286° C.

Mass Spectrum (CI): m/e 347 (M⁺ +1), 329 (M⁺ --OH), 302 (M⁺ --CO₂).

Nuclear Magnetic Resonance Spectrum (hexadeuterated dimethyl sulfoxide, δ ppm): 0.8-1.2 (4H, multiplier); 3.92 (1H, multiplier); 7.05 (1H, triplet, J=73 Hz); 7.92 (2H, broad singlet); 8.62 (1H, singlet); 14.25 (1H, singlet).

Elemental analysis: Calculated for C₁₄ H₁₀ F₄ N₂ O₄ : C, 48.57%; H, 2.91%; N, 8.09%. Found: C, 48.45%; H, 2.53%; N, 8.03%.

PREPARATION 12

5-Amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid boron difluoride chelate [(IX), R¹ =--OCHF₂, R³ =NH₂, X=F]

0.96 g of boron trifluoride.diethyl etherate was added to a mixture of 1.17 g (0.0034 mole) of 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid [(XXI), R¹ =--OCHF₂, R³ =NH₂, X=F, or (VI), R¹ =--OCHF₂, R³ =NH₂, R¹³ =H, X=F] (prepared as described in Preparation 11) and 30 ml of methyl isobutyl ketone, and the mixture was heated under reflux for 6 hours. At the end of this time, the mixture was cooled with ice, and the crystals which precipitated from the reaction mixture were collected by filtration and washed with diethyl ether to afford 1.29 g of 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid boron difluoride chelate as yellow crystals, melting at not less than 300° C.

Mass Spectrum (CI): m/e 395 (M⁺ +1).

Elemental analysis: Calculated for C₁₄ H₉ BF₆ N₂ O₄ : C, 42.68%; H. 2.30%; N. 7.11%. Found: C, 42.29%; H. 2.30%; N. 7.08%.

PREPARATION 13

2,4,5-Trifluoro-3-hydroxybenzoic acid [(XXIII), X=X'=F]

2700 g of 3,5,6-trifluoro-4-hydroxyphthalic acid and 6 liters of water were placed in an autoclave, and the mixture was heated at 140° C for 3 hours in an atmosphere of nitrogen. At the end of this time, the reaction mixture was cooled to room temperature and concentrated by evaporation under reduced pressure, to precipitate crystals, which were collected by filtration, washed with chloroform and dried to give 1623 g of 2,4,5-trifluoro-3-hydroxybenzoic acid [(XXIII), X =X'=F] as a colorless powder, melting at 144°-146° C.

Mass Spectrum: m/e 192 (M⁺).

Nuclear Magnetic Resonance Spectrum (CD₃ OD, δ ppm): 4.94 (1H, broad singlet); 7.25 (1H, multiplier).

PREPARATION 14 (2S)-Methylpiperazine

14(a) Ethyl N-cyanomethyl-L-alanate

10 ml of water, followed by 3.2 g (0.065 mole) of Sodium cyanide, were added to 10 g (0.065 mole) of ethyl L-alanate hydrochloride. 5.3 g (0.065 mole) of a solution of 37% by weight of formaldehyde in water were then added dropwise to the mixture. During this addition, the reaction temperature increased to nearly 40° C. The resulting mixture was then stirred at room temperature for 6 hours, after which it was allowed to stand overnight at the same temperature. The reaction mixture was then extracted with methylene chloride, and the organic extract was washed with a saturated aqueous solution of sodium bicarbonate and with water, in that order. It was then dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel, using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 5.6 g of ethyl N-cyanomethyl-L-alanate as a colorless oil.

Mass Spectrum (CI): m/e 157 (M⁺ +1), 130 (M⁺ --CN).

Nuclear Magnetic Resonance Spectrum (CDCl₃) δ ppm: 1.28 (3H, triplet, J=6 Hz); 1.33 (3H, doublet, J=6 Hz); 2.15 (1H, singlet); 3.45 (1H, quartet, J=6 Hz); 3.60 (2H, singlet; 4.20 (2H, quartet, J=6 Hz).

14(b) (3S)-Methyl-2-oxopiperazine

A mixture of 5.0 g (0.321 mole) of ethyl N-cyano-methyl-L-alanate [prepared as described in step (a) above], 56 g of ethanol containing 4% w/w ammonia and 1.38 g of Raney nickel was transferred to an autoclave where it was then stirred under a hydrogen pressure of 50 kg/cm² at 90° C. for 2 hours. At the end of this time, the catalyst was removed by filtration and the solvent was stripped from the filtrate by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 1:20 by volume mixture of methanol and chloroform as the eluent, to afford 2.8 g of (3S)-methyl-2-oxopiperazine as colorless crystals.

Mass Spectrum (CI): m/e 115 (M⁺ +1).

Nuclear Magnetic Resonance Spectrum (CDCl₃) δ ppm: 1.40 (3H, doublet, J=6 Hz); 1.78 (1H, singlet); 2.9-3.6 (5H, multiplet); 7.00 (1H, broad).

14(c) (2S)-Methyl piperazine

A solution of 2.29 g (0.020 mole) of (3S)-methyl-2-oxopiperazine [prepared as described in step (b) above] in 35 ml of tetrahydrofuran was added dropwise to a suspension of 1.53 g (0.040 mole) of lithium aluminum hydride in 35 ml of tetrahydrofuran, and the mixture was heated under reflux for 5 hours. It was then allowed to cool, after which a small amount of water was added to the reaction mixture, whilst ice-cooling, to decompose any excess of the reducing agent. The reaction mixture was then filtered, and the filtrate was mixed with 10 ml of concentrated aqueous hydrochloric acid and evaporated to dryness under reduced pressure. The residue was triturated with a mixture of diethyl ether and ethanol to give 2.73 g of (2S)-methylpiperazine dihydrochloride as a colorless powder, which was dissolved in 10 ml of water. The pH of the aqueous solution was adjusted to a value greater than 10 by the addition of a 10% w/v aqueous solution of sodium hydroxide, and then the mixture was extracted with chloroform. The chloroform extract was dried over anhydrous sodium sulfate and the solvent was removed by evaporation under reduced pressure. 1.30 g of (2S)-methylpiperazine was obtained as colorless needles by vacuum distillation of the residue. It was determined by high pressure liquid chromatography analysis [using GITC (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate) derivatives] that the product was an S-isomer having an optical purity of 98.5%.

Mass Spectrum (CI): m/e 101 (M⁺ +1).

Nuclear Magnetic Resonance Spectrum (CDCl₃) δ ppm: 1.00 (3H, doublet, J=6 Hz); 1.85 (2H, singlet); 2.30-2.45 (1H, multiplier); 2.6-3.0 (6H, multiplier).

PREPARATIONS 15-18

Following a procedure similar to that described in Preparation 14, but using the starting materials listed in Table 2, the following piperazine derivatives were synthesized.

                  TABLE 2     ______________________________________     Preparation             Starting      Product     No.     material      (piperazines)                                        m.p.(°C.)     ______________________________________     15      L-α-aminobutyric                           (2S)-ethyl-  231-234             acid          piperazine 2HCl     16      L-valine      (2S)-isopropyl-                                        261-264                           piperazine 2HCl     17      2-aminoisobutyric                           2,2-dimethyl-                                        229-240             acid          piperazine 2HCl     18      DL-O-methylserine                           DL-2-methoxy-                                        199-204                           methylpiperazine                           2HCl     ______________________________________

PREPARATION 19 (3S)-Aminopyrrolidine dihydrochloride

19(a) Ethyl N-t-butoxycarbonyl-L-aspartate

7.33 g (0.072 mole) of triethylamine were added, whilst ice-cooling, to a solution of 14.88 g (0.066 mole) of ethyl L-aspartate hydrochloride dissolved in 200 ml of methylene chloride. The mixture was then stirred for 20 minutes, after which 14.4 g (0.066 mole) of di-t-butyl dicarbonate were added to it in portions. When the addition was complete, the mixture was stirred for 2 hours and then concentrated by evaporation under reduced pressure. Toluene was added to the residue, and the triethylamine hydrochloride which precipitated was removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel, using a 4:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 18.61 g of ethyl N-t-butoxycarbonyl-L-aspartate as a colorless oil.

Mass Spectrum (CI): m/e 234 (M⁺ +1--CH₂ ═C(CH₃)₂), 190 (M⁺ +1--CO₂ --CH₂ ═C(CH₃)₂).

19(b) (2S)-t-Butoxycarbonylamino-1,4-dihydroxybutane

40 ml of tetrahydrofuran containing 10.0 g (0.035 mole) of ethyl N-t-butoxycarbonyl-L-aspartate [prepared as described in step (a) above] were added dropwise to a solution of 3.01 g (0.138 mole) of lithium borohydride dissolved in 100 ml of tetrahydrofuran. The dropping rate was adjusted so that the reaction temperature was maintained at 40° C. After completion of the addition, the mixture was stirred at room temperature for 4 hours. At the end of this time, any excess of the reducing agent was decomposed by the addition of a small amount of water. The reaction mixture was then filtered, and the filtrate was concentrated by evaporation under reduced pressure, to remove the tetrahydrofuran. Sodium chloride was then added, and the mixture was extracted with ethyl acetate. The organic extract was dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure, to afford 6.15 g of (2S)-t-butoxycarbonylamino-1,4-dihydroxybutane as a colorless oil.

Mass Spectrum (CI): m/e 206 (M⁺ +1 ), 150 (M⁺ +1-CH₂ ═C(CH₃)₂), 106 (M⁺ +1 --CO₂ --CH₂ ═C(CH₃)₂).

9(c) (2S)-t-Butoxycarbonylamino-1,4-di(methylsulfonyloxy)butane

15.12 g (0.132 mole) of methanesulfonyl chloride were added dropwise, whilst ice-cooling, to a solution of 13.0 g (0.060 mole) of (2S)-t-butoxycarbonylamino-1,4-dihydroxybutane [prepared as described in step (b) above] and 14.54 g (0.144 mole) of triethylamine in 250 ml of methylene chloride. The mixture was stirred for 3 hours, whilst ice-cooling, after which it was allowed to stand overnight at room temperature. At the end of this time, it was mixed with water and with methylene chloride. The organic layer was separated and dried over anhydrous sodium sulfate, and then the dried organic layer was concentrated by evaporation under reduced pressure, to give 20.22 g of (2S)-t-butoxycarbonylamino-1,4-di(methylsulfonyloxy)butane as colorless crystals.

Mass Spectrum (CI): m/e 210 (M⁺ --OSO₂ CH₃ --CH₂ ═C(CH₃)₂).

19 (d) (3S)-Aminopyrrolidine dihydrochloride

6.0 g (0.059 mole) of triethylamine were added to a suspension of 20.22 g (0.056 mole) of (2S)-t-butoxycarbonylamino-1,4-di(methylsulfonyloxy)butane [prepared as described in step (c) above] in 130 ml of methanol. Ammonia gas was passed into the mixture until it reached saturation, and the mixture was then stirred at room temperature for 2 days. At the end of this time, it was concentrated by evaporation under reduced pressure. The resulting residue was dissolved in 150 ml of methylene chloride, and then 12.22 g (0.056 mole) of di-t-butyl dicarbonate were added to the resulting solution. 23 ml of triethylamine were then added dropwise, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was then washed with water and dried over anhydrous sodium sulfate, after which it was concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford (3S)-t-butoxycarbonylamino-1-t-butoxycarbonylpyrrolidine as a colorless oil. The oil was mixed with 10 ml of concentrated aqueous hydrochloric acid, and the mixture was evaporated to dryness under reduced pressure, and triturated with ethanol to give 2.87 g of (3S)-aminopyrrolidine dihydrochloride as a colorless powder.

Mass Spectrum (CI): m/e 87 (M⁺ +1), 70 (M⁺ --NH₂).

PREPARATION 20 3-Amino-4-(2,2,2-trifluoroethoxy)pyrrolidine dihydrochloride

20(a) 1-t-Butoxycarbonyl-3-(2,2,2-trifluoroethoxy)4-methylsulfonyloxypyrrolidine

1.08 g (0.027 mole) of a §0% w/w dispersion of sodium hydride in mineral oil was added, whilst cooling with water, to 15 ml of 2,2,2-trifluoroethanol, and the mixture was stirred for 20 minutes. At the end of this time, 5.0 g (0.027 mole) of 1-t-butoxycarbonyl-3,4-epoxypyrrolidine were added to the mixture, which was then heated under reflux for 3 hours. The reaction mixture was then mixed with a saturated aqueous solution of sodium chloride and extracted with ethyl acetate. The organic extract was dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure. The concentrate was dissolved in 50 ml of pyridine, and 3.23 g (0.028 mole) of methanesulfonyl chloride were added, whilst ice-cooling, to the resulting solution. The mixture was then stirred at room temperature for 5 hours and then allowed to stand overnight at room temperature. After it had been diluted with 300 ml of water, the reaction mixture was extracted with toluene. The organic extract was dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 7.07 g of 1-t-butoxycarbonyl-1-3-(2,2,2-trifluoroethoxy)-4-methylsulfonyloxy-pyrrolidine.

20(b) 3-Amino-1-t-butoxycarbonyl-4-(2,2,2-trifluoroethoxy)pyrrolidine

A mixture of 3.95 g (0.011 mole) of 1-t-butoxycarbonyl-3-(2,2,2-trifluoroethoxy)-4-methylsulfonyloxypyrrolidine [prepared as described in step (a) above] and 100 ml of methanol containing 20% w/v ammonia was transferred to an autoclave and then stirred at 140° C. for 10 hours. At the end of this time, the solvent was removed by distillation under reduced pressure, and the residue was mixed with a saturated aqueous solution of sodium carbonate and extracted with ethyl acetate. The organic extract was dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 1:9 by volume mixture of ethanol and ethyl acetate as the eluent to give 1.61 g of 3-amino-1-t-butoxycarbonyl-4-(2,2,2-trifluoroethoxy)pyrrolidine as a colorless oil.

Mass Spectrum (CI)- m/e 285 (M⁺ +1). 229 (M⁺ 1--CH₂ ═C(CH₃)₂ ).

20(c) 3-Amino-4-(2,2,2-trifluoroethoxy)pyrrolidine dihydrochloride

A mixture of 1.61 g (0.006 mole) of 3-amino-1-t-butoxycarbonyl-1-4-(2,2,2-trifluoroethoxy)pyrrolidine [prepared as described in step (b) above], 30 ml of ethanol, 2 ml of concentrated aqueous hydrochloric acid and 4 ml of water was allowed to stand overnight an room temperature after which in was evaporated to dryness under reduced pressure, to afford 1.60 g of 3-amino-4-(2,2,2-trifluoroethoxy)pyrrolidine dihydrochloride as colorless crystals.

Mass Spectrum (CI): m/e 185 (M⁺ +1).

PREPARATION 21 3-Amino-4-methoxymethylpyrrolidine dihydrochloride

21(a) 1-Benzyl-3-ethoxycarbonyl-4-hydroxyiminopyrrolidine

A solution of 24.7 g (0.1 mole) of 1-benzyl-3-ethoxycarbonyl-4-pyrrolidone in 135 ml of ethanol was added dropwise at room temperature to a solution of 34.7 g (0.5 mole) of hydroxylamine hydrochloride dissolved in 135 ml of water, and then 28.1 g (0.265 mole) of sodium carbonate were added to the mixture. The mixture was then stirred at room temperature for 6.5 hours, after which it was extracted with 300 ml of chloroform. The chloroform extract was washed with water and dried over anhydrous sodium sulfate. It was then concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 2:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 15.8 g of 1-benzyl-3-ethoxycarbonyl-4-hydroxyiminopyrrolidine as a brown oil.

Mass Spectrum (CI): m/e 263 (M⁺ +1).

Infrared Absorption Spectrum (capillary) ν_(max) cm⁻¹ : 3300, 1740.

21(b) 3-Amino-1-benzyl-4-hvdroxymethylpyrrolidine

A solution of 5.24 g (0.02 mole) of 1-benzyl-3-ethoxycarbonyl-4-hydroxyiminopyrrolidine [prepared as described in step (a) above] in 10 ml of toluene was added dropwise to 28 ml of a 3.4M solution of sodium bis(2-methoxyethoxy)aluminum hydride in toluene over a period of 1 hour. The mixture was stirred at room temperature for 1.5 hours and was then heated under reflux for 2 hours. At the end of this time, the reaction mixture was allowed to cool to room temperature, after which ice and water were added to it to form a precipitate, which was removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using methanol as the eluent, to afford 2.16 g of 3-amino-1-benzyl-4-hydroxymethylpyrrolidine as a brown oil.

Mass Spectrum (CI): m/e 207 (M⁺ +1).

Infrared Absorption Spectrum (capillary) ν_(max) cm⁻¹ : 3150-3400.

21(c) 1-Benzyl-3-(N-t-butoxycarbonyl)amino-4-hydroxylmethylpyrrolidine

6.21 g (0.0285 mole) of di-t-butyl dicarbonate were added in portions at room temperature to a solution of 5.87 g (0.0285 mole) of 3-amino-1-benzyl-4-hydroxymethylpyrrolidine [prepared as described in step (b) above] in 100 ml of methylene chloride. The mixture was stirred at room temperature for 1 day and then the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography through silica gel using ethyl acetate as the eluent, to afford 6.32 g of 1-benzyl-3-(N-t-butoxycarbonyl)amino-4-hydroxymethylpyrrolidine as a pale brown oil.

Infrared Absorption Spectrum (capillary) ν_(max) cm⁻¹ : 3350, 1680-1720.

21(d) 3-(N-t-Butoxycarbonyl)amino-4-hydroxymethylpyrrolidine

A mixture of a solution of 6.32 g (0.0207 mole) of 1-benzyl-3-(N-t-butoxycarbonyl)amino-4-hydroxymethylpyrrolidine [prepared as described in step (c) above] dissolved in 100 ml of ethanol and 2.0 g of 20% w/w palladium-on-carbon was transferred to a stainless steel autoclave and stirred at room temperature under a hydrogen pressure of 100 kg/cm² for 27 hours. At the end of this time, the catalyst was removed by filtration, and the filtrate was concentrated by evaporation under reduced pressure, to afford 3.99 g of 3-(N-t-butoxycarbonyl)amino-4-hydroxymethylpyrrolidine as a colorless crystalline oil.

Mass Spectrum (CI): m/e 217 (M⁺ +1).

Infrared Absorption Spectrum (KBr) ν_(max) cm⁻¹ : 3350, 3270, 1680-1690.

21(e) 1-t-Butoxycarbonyl-3-(N-t-butoxycarbonyl)amino-4-hydroxymethylpyrrolidine

3.12 g of di-t-butyl dicarbonate were added in portions at room temperature to a solution of 3.08 g (0.0143 mole) of 3-(N-t-butoxycarbonyl)amino-4-hydroxymethylpyrrolidine [prepared as described in step (d) above] in 50 ml of methylene chloride, and the mixture was stirred at room temperature for one day. At the end of this time, the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel using a 1:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 3.99 g of 1-t-butoxycarbonyl-3-(N-t-butoxycarbonyl)amino-4-hydroxymethylpyrrolidine as colorless crystals.

Mass Spectrum (CI): m/e 317 (M⁺ +1). 21(f) 1-t-Butoxycarbonyl-3-(N-t-butoxycarbonyl)amino-4-methoxymethylpyrrolidine

0.3 ml of boron trifluoride.diethyl etherate was added dropwise to a solution of 3.86 g (0.0122 mole) of 1-t-butoxycarbonyl-3-(N-t-butoxycarbonyl ) amino-4-hydroxymethylpyrrolidine [prepared as described in step (e) above] in 190 ml of diethyl ether cooled with ice, and then an ethereal solution containing 0.126 mole of diazomethane was added to the mixture over a period of 1.5 hours. The mixture was stirred at the same temperature for 0.5 hour, after which it was allowed to stand overnight at room temperature. It was then mixed with a saturated aqueous solution of sodium chloride and the ethereal layer was separated. The ethereal layer was dried, and then the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel using a 2:1 by volume mixture of toluene and ethyl acetate as the eluent to afford 0.47 g of 1-t-butoxycarbonyl-3-(N-t-butoxycarbonyl)amino-4-methoxymethylpyrrolidine as a colorless oil.

Mass Spectrum (CI): m/e 331 (M⁺ +1).

Infrared Absorption Spectrum (capillary) ν_(max) cm⁻¹ : 3330, 1670-1730.

21(g) 3-Amino-4-methoxymethylpyrrolidine dihydrochloride

7 ml of 6N aqueous hydrochloric acid were added to a solution of 0.58 g (0.0021 mole) of 1-t-butoxycarbonyl-3-(N-t-butoxycarbonyl)amino-4-methoxymethylpyrrolidine [prepared as described in step (f) above] in 30 ml of ethanol. The mixture was then heated under reflux for 2 hours, after which it was evaporated to dryness under reduced pressure to give 0.43 g of 3-amino-4-methoxymethylpyrrolidine dihydrochloride as a brown oil.

Mass Spectrum (CI): m/e 131 (M⁺ +1).

PREPARATION 22 2-Fluoromethylpiperazine dihydrochloride

22(a) N-Benzyl-N-(3-fluoro-2-hydroxypropyl)ethanolamine

A solution of 22.20 g (0.3 mole) of epifluorohydrin and 67.95 g (0.45 mole) of N-benzylethanolamine dissolved in 200 ml of ethanol was heated under reflux for 5 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using ethyl acetate as the eluent, to give 64.93 g of N-benzyl-N-(3-fluoro-2-hydroxypropyl)ethanolamine as a colorless oil.

Mass Spectrum (CI): m/e 228 (M⁺ +1).

22(b) N-(3-Fluoro-2-methylsulfonyloxypropyl)-N-(2-methylsulfonyloxyethyl)benzylamine

7.27 g (0.072 mole) of triethylamine were added to a solution of 6.75 g (0.03 mole) of N-benzyl-N-(3-fluoro-2-hydroxypropyl)ethanolamine [prepared as described in step (a) above] in 200 ml of ethyl acetate. Whilst stirring and ice-cooling the mixture, 8.24 g (0.072 mole) of methanesulfonyl chloride were added to it. After the resulting mixture had been stirred for 3 hours at the same temperature, an aqueous solution of sodium bicarbonate was added to it. The organic layer was separated, washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, to give 12.49 g of N-(3-fluoro-2-methylsulfonyloxypropyl)-N-(2-methylsulfonyloxyethyl)benzylamine as a pale yellow oil.

Mass Spectrum (CI): m/e 384 (M⁺ +1).

22(c) 1,4-Dibenzyl-2-fluoromethylpiperazine

4.82 g (0.045 mole) of benzylamine and 9.09 g (0.09 mole) of triethylamine were added to a solution of N-(3-fluoro-2-methylsulfonyloxypropyl)-N-(2-methylsulfonyloxyethyl)benzylamine [prepared as described in step (b) above] dissolved in 200 ml of ethanol. The mixture was heated under reflux for 2 hours and then concentrated by evaporation under reduced pressure. 100 ml of ethanol and 40 ml of a 2N aqueous solution of sodium hydroxide were added to the residue, and the mixture was concentrated by evaporation under reduced pressure. The residue was mixed with ethyl acetate, and insoluble materials were removed by filtration. The filtrate was freed from the solvent by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using a 9:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 3.60 g of 1,4-dibenzyl-2-fluoromethylpiperazine as a yellow oil.

Mass Spectrum (CI): 299 (M⁺ +1).

22(d) 2-Fluoromethylpiperazine dihydrochloride

A mixture of a solution of 23.85 g (0.08 mole) of 1,4-dibenzyl-2-fluoromethyl piperazine [prepared as described in step (c) above] in 500 ml of methanol and 33 ml of concentrated aqueous, hydrochloric acid was stirred vigorously at room temperature for 1 hour in an atmosphere of hydrogen and in the presence of 1.0 g of 20% w/w palladium-on-carbon. At the end of this time, the catalyst was removed by filtration and washed with water. The filtrate and washings were concentrated by evaporation under reduced pressure, and the residue was dissolved in 200 ml of water. The resulting aqueous solution was washed vigorously with ethyl acetate and separated. The aqueous layer was concentrated by evaporation under reduced pressure, and the residue was washed with ethanol to afford 13.76 g of 2-fluoromethylpiperazine dihydrochloride as a colorless powder, melting at 205°-218° C.

Mass Spectrum (CI): m/e 119 (M⁺ +1).

Elemental analysis: Calculated for C₅ H₁₃ Cl₂ FN₂ : C, 31.43%; H, 6.86%; N, 14.66%. Found: C, 31.42%; H, 6.81%; N, 14.71%.

PREPARATION 23 (2S)-Methylhomopiperazine dihydrochloride

23(a) Ethyl N-cyanoethyl-L-alanate

A solution of 15.3 g (0.131 mole) of ethyl L-alanate, 7.0 g (0.132 mole) of acrylonitrile and 1.0 g (0.018 mole) of sodium methoxide dissolved in 150 ml of ethanol was heated under reflux for 7 hours. After it had been allowed to cool, the reaction mixture was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using a 4:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 12.5 g of ethyl N-cyanoethyl-L-alanate as a colorless oil.

Mass Spectrum (CI): m/e 171 (M⁺ +1).

23(b) (3S)-Methyl-2-oxohomopiperazine

A mixture of 9.8 g (0.057 mole) of ethyl N-cyanoethyl-L-alanate [prepared as described in step (a) above], 70 g of ethanol containing 4% w/w ammonia and 1.79 g of Raney nickel was transferred to an autoclave and then stirred under a hydrogen pressure of 60 kg/cm² at 90° C. for 3 hours. After the mixture had been allowed to cool, the catalyst was removed by filtration and the filtrate was concentrated by evaporation under reduced pressure. The residue was mixed with 200 ml of xylene and 1.4 g of dibutyltin oxide, and the mixture was heated under reflux for 10 hours. A fraction containing ethanol, formed during the reaction, was eliminated from the reaction system. Subsequently, the reaction mixture was concentrated by evaporation under reduced pressure, and the residue was purified by column chromatography through silica gel using a 9:1 by volume mixture of chloroform and methanol as the eluent, to afford 5.3 g of (3S)-methyl-2-oxohomopiperazine as pale brown crystals.

Mass Spectrum (CI): m/e 129 (M⁺ +1).

23(c) (2S)-Methylhomopiperazine dihydrochloride

A mixture of 4.92 g (0.038 mole) of (3S)-methyl-2-oxohomopiperazine [prepared as described in step (b) above] in 60 ml of tetrahydrofuran was added dropwise, whilst ice-cooling, to a suspension of 2.91 g (0.077 mole) of lithium aluminum hydride in 60 ml of tetrahydrofuran, and the mixture was heated under reflux for 5 hours. After the reaction mixture had been allowed to cool, a small amount of water was added to it, whilst ice-cooling, to decompose any excess of the reducing agent. The reaction mixture was then filtered, and 20 ml of concentrated aqueous hydrochloric acid were added to the filtrate, which was then evaporated to dryness under reduced pressure. The residue was triturated with ethanol, to give 5.93 g of (2S)-methylhomopiperazine dihydrochloride as colorless crystals, melting at 211°-220° C.

Mass Spectrum (CI): m/e 115 (M⁺ +1).

PREPARATION 24 2,6-Bis(fluoromethyl)piperazine dihydrochloride

24(a) N,N-Bis(3-fluoro-2-hydroxypropyl)benzylamine

A solution of 27.28 g (0.359 mole) of epifluorohydrin and 19.20 g (0.1795 mole) of benzylamine dissolved in 200 ml of ethanol was heated under reflux for 4 hours. The reaction mixture was then concentrated by evaporation under reduced pressure, to give 46.6 g of N,N-bis(3-fluoro-2-hydroxypropyl)benzylamine as a colorless oil.

Mass Spectrum (CI): m/e 260 (M⁺ +1).

24(b) 1,4-Dibenzyl-2,6-bis(fluoromethyl)piperazine

28.89 g (0.286 mole) of triethylamine were added to a solution of 33.67 g (0.13 mole) of N,N-bis(3-fluoro-2-hydroxypropyl)benzylamine [prepared as described in step (a) above] in 300 ml of tetrahydrofuran. 32.76 g (0.286 mole) of methanesulfonyl chloride were then added dropwise to the mixture, whilst ice-cooling. After the mixture had been stirred at room temperature for 6 hours, 39.40 g (0.39 mole) of triethylamine, 20.87 g (0.195 mole) of benzylamine and 300 ml of ethanol were added to it, and it was then heated under reflux for 3 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure, and 300 ml of water containing 30 g of sodium hydroxide were added to the residue. The aqueous mixture thus obtained was extracted with ethyl acetate and the organic extracts were washed with water, dried over anhydrous sodium sulfate and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography through silica gel using a 20:1 by volume mixture of toluene and ethyl acetate as the eluent, to afford 1,4-dibenzyl-2,6-bis(fluoromethyl)piperazine, including 6.29 g of isomer A and 6.60 g of isomer B, as colorless crystals.

Rf value of isomer A: 0.7

Rf value of isomer B: 0.5

(Thin layer plane: silica gel F₂₅₄. Merck; Developing solvent: a 9:1 by volume mixture of toluene and ethyl acetate)

Mass Spectrum (CI) of both isomers A and B: m/e 331 (M⁺ +1).

24(c) 2,6-Bis(fluoromethyl)piperazine dihydrochloride

A mixture of a suspension of 5.03 g (0.015 mole) of 1,4-dibenzyl-2,6-bis(fluoromethyl)piperazine isomer B [prepared as described in step (b) above] in 130 ml of methanol and 6 ml of concentrated aqueous hydrochloric acid was stirred vigorously under a stream of hydrogen at room temperature for 1 hour in the presence of 0.6 g of 20% w/w palladium-on-carbon. At the end of this time, the catalyst was removed by filtration, and the filtrate was concentrated by evaporation under reduced pressure. The residue was mixed with 50 ml of water, and the resulting insoluble materials were removed by filtration. The filtrate was concentrated by evaporation under reduced pressure, and the residue was washed with ethanol, to afford 3.10 g of 2,6-bis(fluoromethyl)piperazine (isomer B) dihydrochloride as a colorless powder, melting at 207°-225° C.

Mass Spectrum (CI): m/e 151 (M⁺ +1).

Elemental analysis: Calculated for C₆ H₁₄ Cl₂ F₂ N₂ : C, 32.30%; H, 6.32%; N, 12.56%.

Found: C, 32.38%; H, 6.26%; N, 12.60%. The above procedure was repeated but using 1,4-dibenzyl-2,6-bis(fluoromethyl)piperazine (isomer A) to afford 2,6-bis(fluoromethyl)piperazine (isomer A) dihydrochloride as a colorless powder.

Mass Spectrum (CI): m/e 151 (M⁺ +1).

Elemental analysis: Calculated for C₆ H₁₄ Cl₂ F₂ N₂.1/2H₂ O: C, 31.04%; H, 6.51%; N, 12.07%. Found: C, 30.66%; H, 6.22%; N, 11.78%.

EXAMPLE 1

1-Cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

1.63 g (0.016 moles) of 2-methylpiperazine was added to a solution of 2.58 g (0.0068 mole) of 1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid boron difluoride chelate (prepared as described in Preparation 8) in 20 ml of dimethyl sulfoxide, and the mixture was allowed to stand at room temperature overnight. The reaction mixture was then poured into 100 ml of water, and the crystals which precipitated were collected by filtration and washed with water. The crystals were then dissolved in 500 ml of 80% v/v aqueous methanol containing 15 ml of triethylamine, and the solution was heated under reflux for 3 hours. At the end of this time, the solvent was removed by evaporation under reduced pressure, and the residue was washed with ethanol, to give 2.30 g of a pale yellow powder. The whole of this powder was dissolved in 50 ml of water, insoluble materials were removed by filtration, and the filtrate was adjusted to a pH value of 7.5 by the addition of a 1N aqueous solution of sodium hydroxide. The crystals which precipitated were collected by filtration and washed with water and with ethanol, in that order, to give 1.74 g of the title compound as fine pale yellow needles, melting at 223°-225° C.

Mass Spectrum (CI): m/e 412 (M⁺ +1).

Elemental analysis: Calculated for C₁₉ H₂₀ F₃ N₃ O₄ H₂ O: C, 53.14%; H, 5.17%; N, 9.79%. Found: C, 53.44%; H, 4.93%; N, 9.77%.

EXAMPLE 2

1-Cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid hydrochloride

240 ml (0.0024 moles) of 1N aqueous hydrochloric acid were added to a suspension of 1.00 g (0.0024 moles) of 1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (prepared as described in Example 1) in 50 ml of methanol to obtain a transparent solution. This was concentrated by evaporation under reduced pressure, and the residue was washed with ethanol, to give 0.97 g of the title compound (hydrochloride) as a colorless powder, melting at 277°-287° C. (with decomposition).

Elemental analysis: Calculated for C₁₉ H₂₁ ClF₃ N₃ O₄ : C, 50.95%; H, 4.73%; N, 9.38%. Found: C, 50.84%; H, 4.44%; N, 9.29%.

EXAMPLE 3

1-Cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid methanesulfonic acid salt

0.093 g (0.00097 moles) of methanesulfonic acid was added to a suspension of 0.40 g of 1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (prepared as described in Example 1) in 50 ml of methanol to obtain a transparent solution. This was concentrated by evaporation under reduced pressure, and the residue was washed with ethanol, to give 0.47 g of the title compound (methanesulfonic acid salt) as a colorless powder, melting at 289°-292° C. (with decomposition).

Elemental analysis: Calculated for C₂₀ H₂₄ F₃ N₃ O₇ S.1/2H₂ O: C, 46.51%; H, 4.88%; N, 8.14%. Found: C, 46.44%; H, 4.65%; N, 7.97%.

EXAMPLES 4 TO 29

Following a procedure similar to that described in Example 1, 2 or 3, the following compounds were produced.

                  TABLE 3     ______________________________________     Ex    Cpd.     No.   No.    hydrate, salt etc    m.p. (°C.)     ______________________________________      4    34     hydrate              220-221      5    34     hydrochloride, sesquihydrate                                       218-224      6    34     methanesulfonate     282-284                                       (decomp.)      7     5     hydrochloride, sesquihydrate                                       247-251      8    43     hydrate              187-188           cis      9    39     hydrochloride        249-253     10     3     hydrate              240-241           cis     11     3     hydrochloride, hydrate                                       >300           cis    (gradual decomposition from 295)     12     3     methanesulfonate     >300           cis     13    32     hydrochloride, dihydrate                                       213-217     14    45     sesquihydrate        167-170     15     1     hydrate              265-268                                       (decomp.)     16    179    hydrate              251-253                                       (decomp.)     17    148    hydrate              232-237     18    152     --                  226-229     19    188    sesquihydrate        241-245           cis    (decomp.)     20    149     --                  237-241           cis     21    147    hydrate              249-251     22    72     hydrochloride, sesquihydrate                                       230-235     23    59     hydrochloride, hemihydrate                                       252-255     24    73     hydrochloride        228-235                                       (decomp.)     25    46     hydrate              269-271                                       (decomp.)     26    48     hydrate              160-163     27     2     hydrochloride        283-289                  (3-carbon atom of piperazinyl                                       (decomp.)                  is in the R configuration     28     2     hydrochloride        283-286                  (3-carbon atom of piperazinyl                                       (decomp.)                  is in the S configuration     29    56     hydrochloride, sesquihydrate                                       270-275                                       (decomp.)     ______________________________________

EXAMPLE 30

5-Amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3carboxylic acid

1.30 g (0.013 moles) of 2-methylpiperazine was added to a solution of 0.90 g (0.0026 moles) of 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (prepared as described in Preparation 11) in 8 ml of pyridine, and the mixture was stirred at 105°-110° C. for 2 hours. At the end of this time, the solvent was removed by distillation under reduced pressure. Water was added to the residue, and the resulting mixture was neutralized (to about pH 7) by the addition of acetic acid; the mixture was then extracted with chloroform. The extract was washed with water, dried over anhydrous sodium sulfate, and concentrated by evaporation under reduced pressure. The resulting residue was washed with ethanol to give 0.72 g of 5-amino-1-cyclopropyl-S-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid as a yellow powder, melting at 283°-286° C.

Elemental analysis: Calculated for C₁₉ H₂₁ F₃ N₄ O₄ : C, 53.52%; H, 4.96%; N, 13.14%. Found: C, 53.35%; H, 4.93%; N, 13.00%.

EXAMPLES 31 TO 60

Following a procedure similar to that described in Example 30, the following compounds were obtained.

                  TABLE 4     ______________________________________     Ex    Cpd.     No.   No.    hydrate, salt etc    m.p. (°C.)     ______________________________________     31    107    hemihydrate          242-245     32    74     hemihydrate          282-283     33    78     hemihydrate          >300     34    76     dihydrate            297-300           cis     35    116     --                  244-245           cis     36    76     hydrochloride        >300           cis     37    75     hydrochloride, hemihydrate                                       296-298                                       (decomp.)     38    75     hemihydrate          278-281                  (3-carbon atom of piperazinyl                  is in the R configuration     39    75     sesquihydrate        278-281                  (3-carbon atom of piperazinyl                  is in the S configuration     40    129     --                  275-280                                       (decomp.)     41    93     hydrate              264-266                                       (decomp.)     42    94      --                  274-275                                       (decomp.)     43    139     --                  270-273                                       (decomp.)     44    129    dihydrate            270-275                  (3-carbon atom of piperazinyl                                       (decomp.)                  is in the S configuration     45    109    hydrochloride, hemihydrate                                       257-259     46    82      --                  273-274                                       (decomp.)     47    130     --                  285-291                                       (decomp.)     48    134    hydrochloride        255-259                                       (decomp.)     49    144    hemihydrate          252-256                  (3-carbon atom of diazepinyl                  is in the S configuration     50    131     --                  264-267                  (3-carbon atom of piperazinyl                  is in the S configuration     51    90      --                  254-257                                       (decomp.)     52    143     --                  217-221                                       (decomp.)     53    107     --                  234-238                  (3-carbon atom of piperazinyl                  is in the S configuration     54    79      --                  291-294                                       (decomp.)     55    141     --                  239-242                                       (decomp.)     56    113     --                  242-246                                       (decomp.)     57    137     --                  271-273                                       (decomp.)     58    136     --                  253-257                                       (decomp.)     59    142     --                  263-265                                       (decomp.)     60    284     --                  252-253                                       (decomp.)     ______________________________________

EXAMPLE 61

Magnesium [5-amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylate]

23.0 ml (0.0023 mole) of a 0.1N aqueous solution of sodium hydroxide were added to 1.00 g (0.00234 mole) of 5-amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (prepared as described in Example 30), and the resulting insoluble material was removed by filtration. 0.11 g (0.00115 mole) of anhydrous magnesium chloride was added to the filtrate, and the mixture was stirred at room temperature for 90 minutes. At the end of this time, the resulting precipitate was collected by filtration and washed with water, to give 0.91 g of magnesium [5-amino-1-cyclopropyl-8-difluoromethoxy-6-fluoro-7-(3-methylpiperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylate] as a yellow powder, melting at 291°-293° C. (with decomposition).

Elemental analysis: Calculated for C₃₈ H₄₀ F₆ N₈ O₈ Mg.2H₂ O: C, 50.09%; H, 4.86%; N, 12.29%. Found: C, 50.13%; H, 4.75%; N, 12.19%.

BIOLOGICAL ACTIVITY

The antibacterial activities of a number of compounds of the invention were investigated against a wide variety of bacteria, both Gram-positive and Gram-negative, and the results are shown in the following Tables 5 and 6 in terms of their minimal inhibitory concentrations (μg/ml).

By way of comparison results are also given for the known compound. Norfloxacin, which, for brevity, is identified in the Table as "Compound A". Each compound of the invention is identified by the number of one of the foregoing Examples which illustrates its prepare ion.

                  TABLE 5     ______________________________________     Micro-    Compound of Ex. No.     organism  1       5       30    31    39    A     ______________________________________     Staphylo-            209P   0.05    <0.01 <0.01 <0.01 <0.01 0.2     coccus  56    0.05    <0.01 <0.01 <0.01 <0.01 0.4     aureus  535   0.2     <0.01 0.02  0.02  <0.01 6.2     Entero-             681   0.2     0.05  0.05  0.05  0.05  3.1     coccus     faecalis     Escheri-            NI-    <0.01   <0.01 0.02  <0.01 <0.01 0.2            HJ     chia coli             609   0.4     0.4   0.2   0.2   0.05  3.1     Salmo-        <0.01   ≦0.01                                 ≦0.01                                       ≦0.01                                             ≦0.01                                                   0.1     nella     enteriti-     dis     Kleb-   806   0.05    ≦0.01                                 0.05  0.02  0.02  0.4     siella  846   0.02    ≦0.01                                 0.02  ≦0.01                                             ≦0.01                                                   0.4     pneumo-     niae     ______________________________________     Micro-    Compound of Ex. No.     organism      1       5     30    31    39    A     ______________________________________     Entero-             963   0.1     0.02  0.1   0.05  0.05  0.4     bacter     cloacae     Serratia            1184   0.4     0.1   0.4   0.2   0.2   0.2     marce-     scens     Proteus            1420   ≦0.01                           ≦0.01                                 ≦0.01                                       ≦0.01                                             ≦0.01                                                   0.02     vulgaris     Morgan-            1510   0.1     0.02  0.2   0.1   0.2   0.05     ella     morganii     Pseudo-            1001   0.4     0.4   0.4   0.4   0.2   0.8     monas     aerugin-     osa     ______________________________________ 

We claim:
 1. A compound of the formula ##STR20## wherein R¹ is a fluorinated methoxy group, R^(10a) is a hydrogen atom or a C₁ -C₆ alkyl group and R^(3a) is a hydrogen atom, a nitro group or an amino group.
 2. The compound of claim 1, wherein R^(10a) is a C₁ -C₆ alkyl group.
 3. The compound of claim 2, wherein R¹ is a difluoromethoxy group.
 4. The compound of claim 3, wherein R^(3a) is a hydrogen atom.
 5. The compound of claim 3, wherein R^(3a) is a nitro group.
 6. The compound of claim 3, wherein R^(3a) is an amino group.
 7. The compound of claim 1, wherein R^(10a) is a hydrogen atom.
 8. The compound of claim 7, wherein R¹ is a difluoromethoxy group.
 9. The compound of claim 8, wherein R^(3a) is a hydrogen atom.
 10. The compound of claim 8, wherein R^(3a) is a nitro group.
 11. The compound of claim 8, wherein R^(3a) is an amino group.
 12. A compound of the formula ##STR21## wherein R¹ is a fluorinated methoxy group and R^(3a) is a hydrogen atom or an amino group.
 13. The compound of claim 12, wherein R¹ is a difluoromethoxy group.
 14. The compound of claim 13, wherein R^(3a) is a hydrogen atom.
 15. The compound of claim 13, wherein R^(3a) is an amino group. 